A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043616



Internal ID19132835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32681188..32713061hg38UCSC Ensembl
Innerchr11:32702734..32734607hg19UCSC Ensembl
Innerchr11:32659310..32691183hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3831874
hg1931874
hg1831874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510122
Samples
Known GenesCCDC73
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043616
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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