A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569532



Internal ID16356941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55363385..55364417hg38UCSC Ensembl
Innerchr15:55655583..55656615hg19UCSC Ensembl
Innerchr15:53442875..53443907hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381033
hg191033
hg181033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4546n54
Supporting Variantsnssv843379, nssv843400, nssv843401, nssv843390, nssv843399, nssv843395, nssv843391, nssv843378, nssv843381, nssv843402, nssv843393, nssv843383, nssv843382, nssv843384, nssv843389, nssv843385, nssv843380, nssv843403, nssv843388, nssv843398, nssv843392, nssv843396, nssv843386, nssv843394, nssv843397, nssv843387
Samples
Known GenesCCPG1, DYX1C1-CCPG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569532
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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