A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010273



Internal ID19099491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21158626..21176060hg38UCSC Ensembl
Innerchr4:21160249..21177683hg19UCSC Ensembl
Innerchr4:20769347..20786781hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3817435
hg1917435
hg1817435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619889
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)nsv1010273
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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