A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6883



Internal ID15190295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9615340..9631532hg38UCSC Ensembl
Outerchr1:9675398..9691590hg19UCSC Ensembl
Outerchr1:9597985..9614177hg18UCSC Ensembl
Outerchr1:9609664..9625856hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387455
hg197455
hg187455
hg177455
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2187
Supporting Variants
SamplesNA12156
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)nssv6883
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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