A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625030



Internal ID18923311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38235456..38261648hg38UCSC Ensembl
Innerchr4:38237077..38263269hg19UCSC Ensembl
Innerchr4:37913472..37939664hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3826193
hg1926193
hg1826193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012627
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)nssv3625030
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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