A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1808



Internal ID15194406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133306453..133325946hg38UCSC Ensembl
Outerchr9:136181849..136192783hg19UCSC Ensembl
Outerchr9:135171670..135182604hg18UCSC Ensembl
Outerchr9:133211403..133222337hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388810
hg198810
hg188810
hg178810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6749
Supporting Variants
SamplesNA18555
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)nssv1808
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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