A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7547



Internal ID15205881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109978521..110023780hg38UCSC Ensembl
Outerchr10:111738279..111783538hg19UCSC Ensembl
Outerchr10:111728269..111773528hg18UCSC Ensembl
Outerchr10:111728269..111773528hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3845260
hg1945260
hg1845260
hg1745260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8844
SamplesNA12156
Known GenesADD3, ADD3-AS1
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)nsv7547
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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