A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134565



Internal ID19263398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75475980..75476036hg38UCSC Ensembl
Outerchr16:75509878..75509934hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972442
SamplesKWS2
Known GenesCHST6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134565
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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