A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625281



Internal ID18923562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:55646407..55714002hg38UCSC Ensembl
Innerchr4:56512574..56580169hg19UCSC Ensembl
Innerchr4:56207331..56274926hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3867596
hg1967596
hg1867596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006944
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625281
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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