A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737705



Internal ID19035986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18931048..18986746hg38UCSC Ensembl
Innerchr4:18932671..18988369hg19UCSC Ensembl
Innerchr4:18541769..18597467hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3855699
hg1955699
hg1855699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006775
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)nssv3737705
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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