A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107847



Internal ID22017081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100184978..102378892hg38UCSC Ensembl
chr7:99782601..102019339hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382193915
hg192236739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574952
Samples
Known GenesACHE, ACTL6B, AGFG2, AP1S1, C7orf61, CLDN15, COL26A1, CUX1, EPHB4, EPO, FBXO24, FIS1, GATS, GIGYF1, GNB2, LINC01007, LOC100289561, LOC100630923, LRCH4, MEPCE, MIR4285, MIR4653, MIR6840, MIR6875, MOGAT3, MOSPD3, MUC12, MUC17, MYL10, NAT16, NYAP1, PCOLCE, PCOLCE-AS1, PILRA, PILRB, PLOD3, PMS2P1, POP7, PPP1R35, PVRIG, PVRIG2P, RABL5, SAP25, SERPINE1, SH2B2, SLC12A9, SPDYE3, SPDYE6, SRRT, STAG3, STAG3L5P, STAG3L5P-PVRIG2P-PILRB, TFR2, TRIM56, TRIP6, TSC22D4, UFSP1, VGF, ZAN, ZCWPW1, ZNHIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107847
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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