A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613710



Internal ID16054433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17904498..17911472hg38UCSC Ensembl
Innerchr9:17904496..17911470hg19UCSC Ensembl
Innerchr9:17894496..17901470hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg386975
hg196975
hg186975
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129344, nssv1129345, nssv1129346, nssv1129348, nssv1129342, nssv1129341, nssv1129349, nssv1129340, nssv1129347, nssv1129343
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613710
Frequency
Sample Size17421
Observed Gain2
Observed Loss8
Observed Complex0
Frequencyn/a


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