A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519849



Internal ID15100456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113349127..113382693hg38UCSC Ensembl
Innerchr9:116111407..116144973hg19UCSC Ensembl
Innerchr9:115151228..115184794hg18UCSC Ensembl
Innerchr9:113190961..113224527hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3833567
hg1933567
hg1833567
hg1733567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684748, nssv681147, nssv659065
Samples
Known GenesBSPRY, HDHD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519849
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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