A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965521



Internal ID18890190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89454897..89455110hg38UCSC Ensembl
Outerchr16:89521305..89521518hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121519
Supporting Variants
SamplesKWS2
Known GenesANKRD11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965521
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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