A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134561



Internal ID19257031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:72719393..72719698hg38UCSC Ensembl
Outerchr16:72753292..72753597hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991036, nssv3954846
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134561
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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