A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965476



Internal ID18881293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:43887987..43888354hg38UCSC Ensembl
Outerchr11:43909537..43909904hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121475
Supporting Variants
SamplesKWS2
Known GenesALKBH3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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