A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971621



Internal ID18890906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:24926328..24926386hg38UCSC Ensembl
Outerchr16:24937649..24937707hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123021
Supporting Variants
SamplesKWS2
Known GenesARHGAP17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971621
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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