A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967821



Internal ID19233059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:84648394..84648794hg38UCSC Ensembl
Outerchr16:84682000..84682400hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131117
Supporting Variants
SamplesKWS2
Known GenesKLHL36
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967821
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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