A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245703



Internal ID21304360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136595624..136630274hg38UCSC Ensembl
Outerchr4:136590928..136647107hg38UCSC Ensembl
Innerchr4:137516779..137551429hg19UCSC Ensembl
Outerchr4:137512083..137568262hg19UCSC Ensembl
Innerchr4:137736229..137770879hg18UCSC Ensembl
Outerchr4:137731533..137787712hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3856180
hg1956180
hg1856180
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169983
Supporting Variants
SamplesNGO_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245703
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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