A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614920



Internal ID16402329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96160517..96174322hg38UCSC Ensembl
Innerchr9:98922799..98936604hg19UCSC Ensembl
Innerchr9:97962620..97976425hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3813806
hg1913806
hg1813806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176000
SamplesNINDS_158
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614920
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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