A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10568



Internal ID15542230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:99349505..99373187hg38UCSC Ensembl
Outerchr7:98947128..98970810hg19UCSC Ensembl
Outerchr7:98785064..98808746hg18UCSC Ensembl
Outerchr7:98591779..98615461hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3815826
hg1915826
hg1815826
hg1715826
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863
Supporting Variants
SamplesNA18956
Known GenesARPC1A
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)nssv10568
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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