A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5761



Internal ID15543649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:108337422..108450046hg38UCSC Ensembl
Outerchr1:108880044..108992668hg19UCSC Ensembl
Outerchr1:108681567..108794191hg18UCSC Ensembl
Outerchr1:108592086..108704710hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38112625
hg19112625
hg18112625
hg17112625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2276
Supporting Variants
SamplesNA19129
Known Genes
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)nssv5761
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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