A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4777



Internal ID15196490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161443623..161496403hg38UCSC Ensembl
Outerchr1:161413602..161466193hg19UCSC Ensembl
Outerchr1:159680037..159732817hg18UCSC Ensembl
Outerchr1:158226486..158279248hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3852781
hg1952592
hg1852781
hg1752763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3243
Supporting Variants
SamplesNA19129
Known Genes
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)nssv4777
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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