A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969881



Internal ID19244692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:57218709..57219032hg38UCSC Ensembl
Outerchr16:57252621..57252944hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113812
Supporting Variants
SamplesKWS2
Known GenesRSPRY1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969881
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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