A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737709



Internal ID19035990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19609444..19653693hg38UCSC Ensembl
Innerchr4:19611067..19655316hg19UCSC Ensembl
Innerchr4:19220165..19264414hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3844250
hg1944250
hg1844250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013517
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737709
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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