A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620638



Internal ID18918919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31441572..31468327hg38UCSC Ensembl
Innerchr4:31443194..31469949hg19UCSC Ensembl
Innerchr4:31052292..31079047hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3826756
hg1926756
hg1826756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001760
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)nssv3620638
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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