A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984574



Internal ID12630538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7083618..7103531hg38UCSC Ensembl
Innerchr19:7083629..7103542hg19UCSC Ensembl
Innerchr19:7034629..7054542hg18UCSC Ensembl
Innerchr19:7034629..7054542hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819914
hg1919914
hg1819914
hg1719914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751809
Supporting Variants
SamplesBEC_720
Known GenesZNF557
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984574
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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