A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641177



Internal ID18592772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137999933..138081308hg38UCSC Ensembl
Innerchr4:138921087..139002462hg19UCSC Ensembl
Innerchr4:139140537..139221912hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3881376
hg1981376
hg1881376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033022
Supporting Variants
Samples
Known GenesLINC00616
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641177
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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