A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997015



Internal ID17289967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133820279..133963478hg38UCSC Ensembl
Outerchr9:136685401..136828600hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38143200
hg19143200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951803
Supporting Variants
SamplesBILGI_BIOE
Known GenesVAV2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997015
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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