A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569700



Internal ID16357109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63371212..63398345hg38UCSC Ensembl
Innerchr15:63663411..63690544hg19UCSC Ensembl
Innerchr15:61450464..61477597hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3827134
hg1927134
hg1827134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149232
Samples1780862040_A
Known GenesCA12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569700
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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