A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4788



Internal ID15196469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:150945862..150969964hg38UCSC Ensembl
Outerchr4:151867014..151891116hg19UCSC Ensembl
Outerchr4:152086464..152110566hg18UCSC Ensembl
Outerchr4:152224619..152248721hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3824103
hg1924103
hg1824103
hg1724103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4548
Supporting Variants
SamplesNA19129
Known GenesLRBA
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)nssv4788
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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