A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655630



Internal ID18953911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67257116..67376926hg38UCSC Ensembl
Innerchr7:66722103..66841913hg19UCSC Ensembl
Innerchr7:66359538..66479348hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38119811
hg19119811
hg18119811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027702
Supporting Variants
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655630
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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