A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969828



Internal ID18888506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15775407..15775457hg38UCSC Ensembl
Outerchr16:15869264..15869314hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113760
Supporting Variants
SamplesKWS2
Known GenesMYH11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969828
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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