A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101547



Internal ID22010780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98453223..101264028hg38UCSC Ensembl
chr7:98082535..100907309hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382810806
hg192824775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574440
Samples
Known GenesACHE, ACTL6B, AGFG2, AP1S1, AP4M1, ARPC1A, ARPC1B, ATP5J2, ATP5J2-PTCD1, AZGP1, AZGP1P1, BUD31, C7orf43, C7orf61, CLDN15, CNPY4, COPS6, CPSF4, CYP3A4, CYP3A43, CYP3A5, CYP3A7, CYP3A7-CYP3AP1, EPHB4, EPO, FAM200A, FBXO24, FIS1, GAL3ST4, GATS, GIGYF1, GJC3, GNB2, GPC2, KPNA7, LAMTOR4, LOC100289187, LRCH4, MBLAC1, MCM7, MEPCE, MIR106B, MIR25, MIR3609, MIR4653, MIR4658, MIR6840, MIR6875, MIR93, MOGAT3, MOSPD3, MUC12, MUC17, MYH16, NAT16, NPTX2, NYAP1, OR2AE1, PCOLCE, PCOLCE-AS1, PDAP1, PILRA, PILRB, PLOD3, PMS2P1, POP7, PPP1R35, PTCD1, PVRIG, PVRIG2P, SAP25, SERPINE1, SLC12A9, SMURF1, SPDYE3, SRRT, STAG3, STAG3L5P, STAG3L5P-PVRIG2P-PILRB, TAF6, TFR2, TMEM130, TRIM4, TRIM56, TRIP6, TRRAP, TSC22D4, UFSP1, VGF, ZAN, ZCWPW1, ZKSCAN1, ZKSCAN5, ZNF3, ZNF394, ZNF655, ZNF789, ZNHIT1, ZSCAN21, ZSCAN25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101547
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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