A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635566



Internal ID18933847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179740427..180447834hg38UCSC Ensembl
Innerchr4:180661580..181368987hg19UCSC Ensembl
Innerchr4:180898574..181605981hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38707408
hg19707408
hg18707408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016698
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)nssv3635566
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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