A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001725



Internal ID18744256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73488333..73995207hg38UCSC Ensembl
Innerchr4:74354050..74860924hg19UCSC Ensembl
Innerchr4:74572914..75079788hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38506875
hg19506875
hg18506875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633819
Samples
Known GenesAFM, CXCL1, CXCL6, IL8, LOC728040, PF4, PF4V1, PPBP, RASSF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001725
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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