A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5759



Internal ID15550600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56666132..56712782hg38UCSC Ensembl
Outerchr7:56733825..56780475hg19UCSC Ensembl
Outerchr7:56701319..56747969hg18UCSC Ensembl
Outerchr7:56508034..56554684hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3846651
hg1946651
hg1846651
hg1746651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv636, nssv6131, nssv4983, nssv3534
SamplesNA12156, NA12878, NA19240, NA19129
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)nsv5759
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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