A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056442



Internal ID18798973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6890127..6982686hg38UCSC Ensembl
Innerchr19:6890138..6982697hg19UCSC Ensembl
Innerchr19:6841138..6933697hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3892560
hg1992560
hg1892560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723260
Samples
Known GenesEMR1, EMR4P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056442
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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