A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877



Internal ID15552898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:53449905..53483231hg38UCSC Ensembl
Outerchr1:53915578..53948904hg19UCSC Ensembl
Outerchr1:53688166..53721492hg18UCSC Ensembl
Outerchr1:53627599..53660925hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg386108
hg196108
hg186108
hg176108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9140
SamplesNA12156
Known GenesDMRTB1
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)nsv877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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