A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7112



Internal ID15536752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107174142..107217260hg38UCSC Ensembl
Outerchr4:108095299..108138417hg19UCSC Ensembl
Outerchr4:108314748..108357866hg18UCSC Ensembl
Outerchr4:108452903..108496021hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3843119
hg1943119
hg1843119
hg1743119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4455
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)nssv7112
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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