A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564621



Internal ID18516216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6885300..7108040hg38UCSC Ensembl
Innerchr19:6885311..7108051hg19UCSC Ensembl
Innerchr19:6836311..7059051hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38222741
hg19222741
hg18222741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057989
Supporting Variants
Samples
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564621
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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