A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7610



Internal ID15552637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:128451400..128479327hg38UCSC Ensembl
Outerchr10:130249664..130277591hg19UCSC Ensembl
Outerchr10:130139654..130167581hg18UCSC Ensembl
Outerchr10:130139654..130167581hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817586
hg1917586
hg1817586
hg1717586
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3907, nssv6425, nssv1914, nssv972, nssv5327, nssv11245
SamplesNA12156, NA12878, NA15510, NA18555, NA19240, NA19129
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)nsv7610
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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