A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985620



Internal ID18871828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:114526438..114526508hg38UCSC Ensembl
Outerchr11:114397160..114397230hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122668
Supporting Variants
SamplesKWS1
Known GenesNXPE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985620
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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