A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2501



Internal ID15200378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:43438429..43474272hg38UCSC Ensembl
Outerchr19:43942581..43978424hg19UCSC Ensembl
Outerchr19:48634421..48670264hg18UCSC Ensembl
Outerchr19:48634421..48670264hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3835844
hg1935844
hg1835844
hg1735844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7444
SamplesNA12156
Known GenesLYPD3
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)nsv2501
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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