A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252238



Internal ID21302729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121361313..121364161hg38UCSC Ensembl
Outerchr4:121360818..121369976hg38UCSC Ensembl
Innerchr4:122282468..122285316hg19UCSC Ensembl
Outerchr4:122281973..122291131hg19UCSC Ensembl
Innerchr4:122501918..122504766hg18UCSC Ensembl
Outerchr4:122501423..122510581hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg389159
hg199159
hg189159
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170082
Supporting Variants
SamplesMLY_17
Known GenesQRFPR
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252238
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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