A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11148



Internal ID15192745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76513281..76553042hg38UCSC Ensembl
Outerchr7:76142598..76182359hg19UCSC Ensembl
Outerchr7:75980534..76020295hg18UCSC Ensembl
Outerchr7:75787249..75827010hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3839762
hg1939762
hg1839762
hg1739762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5797
Supporting Variants
SamplesNA15510
Known GenesLOC100133091, 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)nssv11148
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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