A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649283



Internal ID18947564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176904803..176968410hg38UCSC Ensembl
Innerchr5:176331804..176395411hg19UCSC Ensembl
Innerchr5:176264410..176328017hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3863608
hg1963608
hg1863608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016283
Supporting Variants
Samples
Known GenesUIMC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649283
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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