A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6041



Internal ID15537823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:176957379..176966474hg38UCSC Ensembl
Outerchr5:176384380..176393475hg19UCSC Ensembl
Outerchr5:176316986..176326081hg18UCSC Ensembl
Outerchr5:176316986..176326081hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg389096
hg199096
hg189096
hg179096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5145
Supporting Variants
SamplesNA12156
Known GenesUIMC1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv6041
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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