A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954481



Internal ID19205266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67329410..67329474hg38UCSC Ensembl
Outerchr16:67363313..67363377hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116155
Supporting Variants
SamplesKWS1
Known GenesLRRC36
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954481
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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