A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7577



Internal ID15552600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:121662932..121704189hg38UCSC Ensembl
Outerchr10:123422446..123463703hg19UCSC Ensembl
Outerchr10:123412436..123453693hg18UCSC Ensembl
Outerchr10:123412436..123453693hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3841258
hg1941258
hg1841258
hg1741258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6421
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)nsv7577
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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