A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3957



Internal ID15548618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:116268103..116313778hg38UCSC Ensembl
Outerchr3:115986950..116032625hg19UCSC Ensembl
Outerchr3:117469640..117515315hg18UCSC Ensembl
Outerchr3:117469640..117515315hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3845676
hg1945676
hg1845676
hg1745676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2409
SamplesNA18555
Known GenesLSAMP
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)nsv3957
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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