A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005221



Internal ID19094438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21785079..21820377hg38UCSC Ensembl
Innerchr4:21786702..21822000hg19UCSC Ensembl
Innerchr4:21395800..21431098hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3835299
hg1935299
hg1835299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619910
Samples
Known GenesKCNIP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005221
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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