A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696140



Internal ID18994421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64818927hg38UCSC Ensembl
Innerchr9:69505934..69831345hg19UCSC Ensembl
Innerchr9:68795754..69121165hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38325412
hg19325412
hg18325412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032458
Supporting Variants
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696140
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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