A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3677



Internal ID15548310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:176843321..176888685hg38UCSC Ensembl
Outerchr1:176812457..176857821hg19UCSC Ensembl
Outerchr1:175079080..175124444hg18UCSC Ensembl
Outerchr1:173544114..173589478hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3845365
hg1945365
hg1845365
hg1745365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7142
SamplesNA12156
Known GenesASTN1
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)nsv3677
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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