A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9296



Internal ID15193561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:61930051..61988763hg38UCSC Ensembl
Outerchr1:62395723..62454435hg19UCSC Ensembl
Outerchr1:62168311..62227023hg18UCSC Ensembl
Outerchr1:62107744..62166456hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3858713
hg1958713
hg1858713
hg1758713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1110
Supporting Variants
SamplesNA18517
Known GenesINADL
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)nssv9296
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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