A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4924



Internal ID15196227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:207353427..207382324hg38UCSC Ensembl
Outerchr1:207526772..207555669hg19UCSC Ensembl
Outerchr1:205593395..205622292hg18UCSC Ensembl
Outerchr1:203915167..203944064hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3828898
hg1928898
hg1828898
hg1728898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4221
Supporting Variants
SamplesNA19129
Known GenesCD55
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)nssv4924
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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