A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7122



Internal ID15536742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:145992631..146030801hg38UCSC Ensembl
Outerchr4:146913783..146951953hg19UCSC Ensembl
Outerchr4:147133233..147171403hg18UCSC Ensembl
Outerchr4:147271388..147309558hg17UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3838171
hg1938171
hg1838171
hg1738171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4535
Supporting Variants
SamplesNA12156
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)nssv7122
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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