A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987415



Internal ID12629234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20638696..20802619hg38UCSC Ensembl
Innerchr19:20821502..20985425hg19UCSC Ensembl
Innerchr19:20613342..20777265hg18UCSC Ensembl
Innerchr19:20613342..20777265hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38163924
hg19163924
hg18163924
hg17163924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751782
Supporting Variants
SamplesBEC_626
Known GenesZNF626
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987415
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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