A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7516



Internal ID15205847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99676637..99708437hg38UCSC Ensembl
Outerchr10:101436394..101468194hg19UCSC Ensembl
Outerchr10:101426384..101458184hg18UCSC Ensembl
Outerchr10:101426384..101458184hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3831801
hg1931801
hg1831801
hg1731801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8835
SamplesNA12156
Known GenesENTPD7
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)nsv7516
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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