A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7521



Internal ID15552539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:100676894..100721523hg38UCSC Ensembl
Outerchr10:102436651..102481280hg19UCSC Ensembl
Outerchr10:102426641..102471270hg18UCSC Ensembl
Outerchr10:102426641..102471270hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3844630
hg1944630
hg1844630
hg1744630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8836
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)nsv7521
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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