A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516318



Internal ID15443611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115578537..115586676hg38UCSC Ensembl
Innerchr9:118340816..118348955hg19UCSC Ensembl
Innerchr9:117380637..117388776hg18UCSC Ensembl
Innerchr9:115420370..115428509hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg388140
hg198140
hg188140
hg178140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652763, nssv680686, nssv691548, nssv669082
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516318
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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