A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5741



Internal ID15550581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:51487684..51560784hg38UCSC Ensembl
Outerchr7:51555381..51628481hg19UCSC Ensembl
Outerchr7:51522875..51595975hg18UCSC Ensembl
Outerchr7:51329590..51402690hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3873101
hg1973101
hg1873101
hg1773101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528, nssv6126, nssv2649
SamplesNA12156, NA12878, 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)nsv5741
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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