A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115220



Internal ID19283499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107563376..107563461hg38UCSC Ensembl
Outerchr9:110325657..110325742hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976275
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115220
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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