A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7265



Internal ID15205571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77017518..77062183hg38UCSC Ensembl
Outerchr10:78777276..78821941hg19UCSC Ensembl
Outerchr10:78447282..78491947hg18UCSC Ensembl
Outerchr10:78447282..78491947hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3844666
hg1944666
hg1844666
hg1744666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8816
SamplesNA12156
Known GenesKCNMA1
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)nsv7265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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