A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002353



Internal ID19091570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21516422..21573590hg38UCSC Ensembl
Innerchr4:21518045..21575213hg19UCSC Ensembl
Innerchr4:21127143..21184311hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3857169
hg1957169
hg1857169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5153n100
Supporting Variantsnssv3619903, nssv3619904
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)nsv1002353
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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