A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5758



Internal ID15550599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56569528..56637640hg38UCSC Ensembl
Outerchr7:56637221..56705333hg19UCSC Ensembl
Outerchr7:56604715..56672827hg18UCSC Ensembl
Outerchr7:56411430..56479542hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3868113
hg1968113
hg1868113
hg1768113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4982, nssv8380, nssv635
SamplesNA12156, 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)nsv5758
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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