A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574952



Internal ID21766995
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 StatusS
Merged Variantsnsv6107847
Supporting Variants
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)nssv17574952
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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