A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5797



Internal ID15203956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76504446..76561016hg38UCSC Ensembl
Outerchr7:76133763..76190333hg19UCSC Ensembl
Outerchr7:75971699..76028269hg18UCSC Ensembl
Outerchr7:75778414..75834984hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3856571
hg1956571
hg1856571
hg1756571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11148, nssv4995, nssv6147, nssv649
SamplesNA12156, NA15510, NA19240, NA19129
Known GenesDTX2, LOC100133091, UPK3B
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)nsv5797
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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