A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7165



Internal ID15205461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:74494436..74523578hg38UCSC Ensembl
Outerchr10:76254194..76283336hg19UCSC Ensembl
Outerchr10:75924200..75953342hg18UCSC Ensembl
Outerchr10:75924200..75953342hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3810366
hg1910366
hg1810366
hg1710366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10765
SamplesNA18956
Known GenesADK
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)nsv7165
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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