A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv446



Internal ID15202485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94960555..95005748hg38UCSC Ensembl
Outerchr11:94693720..94738912hg19UCSC Ensembl
Outerchr11:94333368..94378560hg18UCSC Ensembl
Outerchr11:94333368..94378560hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3845194
hg1945193
hg1845193
hg1745193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8952
SamplesNA12156
Known GenesCWC15, KDM4D
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)nsv446
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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