A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112702



Internal ID19261160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:20439887..20464787hg38UCSC Ensembl
Outerchr17:20343200..20368100hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3824901
hg1924901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967189
SamplesKWS2
Known GenesLGALS9B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112702
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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