A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243



Internal ID15551133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:30936387..30964776hg38UCSC Ensembl
Outerchr10:31225316..31253705hg19UCSC Ensembl
Outerchr10:31265322..31293711hg18UCSC Ensembl
Outerchr10:31265322..31293711hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3828390
hg1928390
hg1828390
hg1728390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6345
SamplesNA12156
Known GenesZNF438
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)nsv6243
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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