A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025506



Internal ID19114724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134892039..134935454hg38UCSC Ensembl
Innerchr4:135813194..135856609hg19UCSC Ensembl
Innerchr4:136032644..136076059hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3843416
hg1943416
hg1843416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641105
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)nsv1025506
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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