A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10785



Internal ID15542013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:30639933..30668630hg38UCSC Ensembl
Outerchr1:31112780..31141477hg19UCSC Ensembl
Outerchr1:30885367..30914064hg18UCSC Ensembl
Outerchr1:30781873..30810570hg17UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3810806
hg1910806
hg1810806
hg1710806
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7679
Supporting Variants
SamplesNA18956
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)nssv10785
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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