A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357



Internal ID15551258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:115727776..115772559hg38UCSC Ensembl
Outerchr8:116740002..116784785hg19UCSC Ensembl
Outerchr8:116809176..116853960hg18UCSC Ensembl
Outerchr8:116809176..116853960hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3844784
hg1944784
hg1844785
hg1744785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8542
SamplesNA12156
Known GenesMIR6507
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)nsv6357
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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