A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4137



Internal ID15548816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178420749..178437917hg38UCSC Ensembl
Outerchr3:178138537..178155705hg19UCSC Ensembl
Outerchr3:179621231..179638399hg18UCSC Ensembl
Outerchr3:179621239..179638407hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3822336
hg1922336
hg1822336
hg1722336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10377
SamplesNA18956
Known GenesLINC01014
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)nsv4137
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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