A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249643



Internal ID21307372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115292258..115663627hg38UCSC Ensembl
Outerchr4:115290107..115673943hg38UCSC Ensembl
Innerchr4:116213414..116584783hg19UCSC Ensembl
Outerchr4:116211263..116595099hg19UCSC Ensembl
Innerchr4:116432863..116804232hg18UCSC Ensembl
Outerchr4:116430712..116814548hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38383837
hg19383837
hg18383837
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170118
Supporting Variants
SamplesNGO_34
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249643
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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