A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3507



Internal ID15548123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:36774831..36792270hg38UCSC Ensembl
Outerchr21:38147132..38164571hg19UCSC Ensembl
Outerchr21:37069002..37086441hg18UCSC Ensembl
Outerchr21:37069002..37086441hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3817440
hg1917440
hg1817440
hg1717440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1625
SamplesNA19240
Known GenesHLCS
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)nsv3507
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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