A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7092



Internal ID15190086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68180919..68215902hg38UCSC Ensembl
Outerchr4:69046637..69081620hg19UCSC Ensembl
Outerchr4:68729232..68764215hg18UCSC Ensembl
Outerchr4:68875403..68910386hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3834984
hg1934984
hg1834984
hg1734984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4371
Supporting Variants
SamplesNA12156
Known GenesFTLP10, TMPRSS11BNL
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)nssv7092
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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