A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6121



Internal ID15191057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:35614529..35660383hg38UCSC Ensembl
Outerchr7:35654139..35699993hg19UCSC Ensembl
Outerchr7:35620664..35666518hg18UCSC Ensembl
Outerchr7:35427379..35473233hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3845855
hg1945855
hg1845855
hg1745855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697
Supporting Variants
SamplesNA12156
Known GenesHERPUD2
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)nssv6121
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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