A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3751



Internal ID15201706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32088214..32133605hg38UCSC Ensembl
Outerchr3:32129706..32175097hg19UCSC Ensembl
Outerchr3:32104710..32150101hg18UCSC Ensembl
Outerchr3:32104710..32150101hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3845392
hg1945392
hg1845392
hg1745392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7001
SamplesNA12156
Known GenesGPD1L
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)nsv3751
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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