A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5704



Internal ID15550540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:37596499..37641906hg38UCSC Ensembl
Outerchr7:37636102..37681509hg19UCSC Ensembl
Outerchr7:37602627..37648034hg18UCSC Ensembl
Outerchr7:37409342..37454749hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3845408
hg1945408
hg1845408
hg1745408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6122
SamplesNA12156
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)nsv5704
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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