A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639638



Internal ID18937919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7414033..7470668hg38UCSC Ensembl
Innerchr5:7414146..7470781hg19UCSC Ensembl
Innerchr5:7467146..7523781hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3856636
hg1956636
hg1856636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022891
Supporting Variants
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639638
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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