A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955210



Internal ID19213113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:34161249..34161309hg38UCSC Ensembl
Outerchr16:33963716..33963776hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127491
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955210
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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