A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6770



Internal ID15537093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:95325251..95354857hg38UCSC Ensembl
Outerchr1:95790807..95820413hg19UCSC Ensembl
Outerchr1:95563395..95593001hg18UCSC Ensembl
Outerchr1:95502828..95532434hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg387349
hg197349
hg187349
hg177349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1921
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)nssv6770
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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