A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10307



Internal ID15542491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:15793019..15824085hg38UCSC Ensembl
Outerchr21:17165338..17196404hg19UCSC Ensembl
Outerchr21:16087209..16118275hg18UCSC Ensembl
Outerchr21:16087209..16118275hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg388442
hg198442
hg188442
hg178442
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3461
Supporting Variants
SamplesNA18956
Known GenesUSP25
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)nssv10307
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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