A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996948



Internal ID17289900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98701619..98711718hg38UCSC Ensembl
Outerchr9:101463901..101474000hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950917
Supporting Variants
SamplesBILGI_BIOE
Known GenesGABBR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996948
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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