A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954438



Internal ID18869668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:22897652..22897930hg38UCSC Ensembl
Outerchr16:22908973..22909251hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121161
Supporting Variants
SamplesKWS1
Known GenesHS3ST2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954438
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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