A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6965



Internal ID15551927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24468506..24488652hg38UCSC Ensembl
Outerchr1:24794996..24815142hg19UCSC Ensembl
Outerchr1:24667583..24687729hg18UCSC Ensembl
Outerchr1:24540302..24560448hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3820147
hg1920147
hg1820147
hg1720147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1967
SamplesNA18555
Known GenesNIPAL3
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)nsv6965
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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