A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835



Internal ID15550684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91564395..91622111hg38UCSC Ensembl
Outerchr7:91193710..91251426hg19UCSC Ensembl
Outerchr7:91031646..91089362hg18UCSC Ensembl
Outerchr7:90838361..90896077hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3857717
hg1957717
hg1857717
hg1757717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5002, nssv653, nssv6149, nssv2671, nssv3552, nssv9908
SamplesNA18507, NA12156, NA12878, NA18555, 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)nsv5835
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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