A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635600



Internal ID18933881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182083542..182102600hg38UCSC Ensembl
Innerchr4:183004695..183023753hg19UCSC Ensembl
Innerchr4:183241689..183260747hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3819059
hg1919059
hg1819059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032121
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)nssv3635600
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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