A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6199



Internal ID15204398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28266586..28274275hg38UCSC Ensembl
Outerchr10:28555515..28563204hg19UCSC Ensembl
Outerchr10:28595521..28603210hg18UCSC Ensembl
Outerchr10:28595521..28603210hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg387690
hg197690
hg187690
hg177690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8530
SamplesNA12156
Known GenesMPP7
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)nsv6199
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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