A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062625



Internal ID18805156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33137612..33164246hg38UCSC Ensembl
Innerchr19:33628518..33655152hg19UCSC Ensembl
Innerchr19:38320358..38346992hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3826635
hg1926635
hg1826635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566577
Samples
Known GenesWDR88
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062625
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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