A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170118



Internal ID21314179
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246551, nssv14243301, nssv14247546, nssv14252301, nssv14249643
SamplesNGO_14, NGO_19, NGO_16, NGO_34, NGO_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170118
Frequency
Sample Size93
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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