A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746163



Internal ID18697758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5415764..5452773hg38UCSC Ensembl
Innerchr5:5415877..5452886hg19UCSC Ensembl
Innerchr5:5468877..5505886hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3837010
hg1937010
hg1837010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021802
Supporting Variants
Samples
Known GenesKIAA0947
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746163
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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