A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896



Internal ID15550751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:109758627..109832984hg38UCSC Ensembl
Outerchr7:109398684..109473041hg19UCSC Ensembl
Outerchr7:109185920..109260277hg18UCSC Ensembl
Outerchr7:108992635..109066992hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3874358
hg1974358
hg1874358
hg1774358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8415, nssv676, nssv9445, nssv11158
SamplesNA12156, NA15510, NA18517, NA19240
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)nsv5896
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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