A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7734



Internal ID15552773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31535138..31564792hg38UCSC Ensembl
Outerchr1:32000739..32030393hg19UCSC Ensembl
Outerchr1:31773326..31802980hg18UCSC Ensembl
Outerchr1:31669832..31699486hg17UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg388026
hg198026
hg188026
hg178026
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6550
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)nsv7734
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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