A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056194



Internal ID18798725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6906839..7022132hg38UCSC Ensembl
Innerchr19:6906850..7022143hg19UCSC Ensembl
Innerchr19:6857850..6973143hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38115294
hg19115294
hg18115294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564647
Samples
Known GenesEMR1, EMR4P, FLJ25758
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056194
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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