A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759737



Internal ID19058018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64809880hg38UCSC Ensembl
Innerchr9:69474914..69822298hg19UCSC Ensembl
Innerchr9:68764734..69112118hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38347385
hg19347385
hg18347385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018264
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)nssv3759737
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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