A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7565



Internal ID15552587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117407950..117453018hg38UCSC Ensembl
Outerchr10:119167461..119212529hg19UCSC Ensembl
Outerchr10:119157451..119202519hg18UCSC Ensembl
Outerchr10:119157451..119202519hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3845069
hg1945069
hg1845069
hg1745069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8850
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)nsv7565
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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