A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150153



Internal ID19196727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:32101378..32196979hg38UCSC Ensembl
Outerchr16:32112699..32208300hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3895602
hg1995602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003456
SamplesKWB1
Known GenesHERC2P4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150153
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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