A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4631



Internal ID15202674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:18303007..18335766hg38UCSC Ensembl
Outerchr1:18629501..18662260hg19UCSC Ensembl
Outerchr1:18502088..18534847hg18UCSC Ensembl
Outerchr1:18374807..18407566hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg386682
hg196682
hg186682
hg176682
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6396
SamplesNA12156
Known GenesIGSF21
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)nsv4631
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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