A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613127



Internal ID16400536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2237390..2363874hg38UCSC Ensembl
Innerchr9:2237390..2363874hg19UCSC Ensembl
Innerchr9:2227390..2353874hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38126485
hg19126485
hg18126485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126215
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613127
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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