A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243060



Internal ID21302850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71080237..71082747hg38UCSC Ensembl
Outerchr4:71079443..71084739hg38UCSC Ensembl
Innerchr4:71945954..71948464hg19UCSC Ensembl
Outerchr4:71945160..71950456hg19UCSC Ensembl
Innerchr4:72164818..72167328hg18UCSC Ensembl
Outerchr4:72164024..72169320hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg385297
hg195297
hg185297
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170309
Supporting Variants
SamplesMLY_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243060
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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