A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646937



Internal ID18945218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106723167..106958172hg38UCSC Ensembl
Innerchr5:106058868..106293873hg19UCSC Ensembl
Innerchr5:106086767..106321772hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38235006
hg19235006
hg18235006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020718
Supporting Variants
Samples
Known GenesLOC102467213
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3646937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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