A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4898



Internal ID15542960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26657106..26703360hg38UCSC Ensembl
Outerchr6:26657334..26703589hg19UCSC Ensembl
Outerchr6:26765313..26811568hg18UCSC Ensembl
Outerchr6:26765313..26811568hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3846255
hg1946256
hg1846256
hg1746256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5231
Supporting Variants
SamplesNA19129
Known GenesZNF322
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)nssv4898
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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