A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4075



Internal ID15548748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:155346096..155392861hg38UCSC Ensembl
Outerchr3:155063885..155110650hg19UCSC Ensembl
Outerchr3:156546579..156593344hg18UCSC Ensembl
Outerchr3:156546587..156593352hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg387662
hg197662
hg187662
hg177662
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7043, nssv2426
SamplesNA12156, NA18555
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)nsv4075
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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