A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7587



Internal ID15552611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:123197262..123228585hg38UCSC Ensembl
Outerchr10:124956778..124988101hg19UCSC Ensembl
Outerchr10:124946768..124978091hg18UCSC Ensembl
Outerchr10:124946768..124978091hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3831324
hg1931324
hg1831324
hg1731324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8856
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)nsv7587
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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