A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7580



Internal ID15205918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122446276..122490980hg38UCSC Ensembl
Outerchr10:124205792..124250496hg19UCSC Ensembl
Outerchr10:124195782..124240486hg18UCSC Ensembl
Outerchr10:124195782..124240486hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3844705
hg1944705
hg1844705
hg1744705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8854
SamplesNA12156
Known GenesARMS2, HTRA1
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)nsv7580
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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