A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755934



Internal ID19054215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37075988..37108977hg38UCSC Ensembl
Innerchr9:37075985..37108974hg19UCSC Ensembl
Innerchr9:37065985..37098974hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3832990
hg1932990
hg1832990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021813
Supporting Variants
Samples
Known GenesLOC100506710
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755934
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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