A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3503



Internal ID15548119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:35533553..35560784hg38UCSC Ensembl
Outerchr21:36905850..36933082hg19UCSC Ensembl
Outerchr21:35827720..35854952hg18UCSC Ensembl
Outerchr21:35827720..35854952hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3827232
hg1927233
hg1827233
hg1727233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7719
SamplesNA12156
Known GenesLOC100506403
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)nsv3503
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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