A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971664



Internal ID19235640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123042734..123042799hg38UCSC Ensembl
Outerchr11:122913442..122913507hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134182
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971664
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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