A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2202



Internal ID15541485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:74913025..74957920hg38UCSC Ensembl
Outerchr18:72624981..72669876hg19UCSC Ensembl
Outerchr18:70753969..70798864hg18UCSC Ensembl
Outerchr18:70753969..70798864hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3844896
hg1944896
hg1844896
hg1744896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2359
Supporting Variants
SamplesNA18555
Known GenesZNF407
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)nssv2202
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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