A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569230



Internal ID16009953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41092451..41191484hg38UCSC Ensembl
Innerchr15:41384649..41483682hg19UCSC Ensembl
Innerchr15:39171941..39270974hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3899034
hg1999034
hg1899034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4499n54
Supporting Variantsnssv842221
Samples
Known GenesEXD1, INO80
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569230
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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