A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738102



Internal ID18689697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:295489..326788hg38UCSC Ensembl
Innerchr4:289278..320577hg19UCSC Ensembl
Innerchr4:279278..310577hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3831300
hg1931300
hg1831300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011981
Supporting Variants
Samples
Known GenesZNF732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738102
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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