A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737699



Internal ID18689294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15774558..15834614hg38UCSC Ensembl
Innerchr4:15776181..15836237hg19UCSC Ensembl
Innerchr4:15385279..15445335hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3860057
hg1960057
hg1860057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010597
Supporting Variants
Samples
Known GenesCD38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737699
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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