A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662187



Internal ID18960468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131331684..131471005hg38UCSC Ensembl
Innerchr7:131016443..131155764hg19UCSC Ensembl
Innerchr7:130666983..130806304hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38139322
hg19139322
hg18139322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017991
Supporting Variants
Samples
Known GenesMKLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662187
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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