A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6769



Internal ID15537094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8719736..8771289hg38UCSC Ensembl
Outerchr19:8830080..8881965hg19UCSC Ensembl
Outerchr19:8691080..8742965hg18UCSC Ensembl
Outerchr19:8691080..8742965hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3851554
hg1951886
hg1851886
hg1751886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2402
Supporting Variants
SamplesNA12156
Known GenesOR2Z1
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)nssv6769
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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