A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988334



Internal ID12635620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22823180..23460655hg38UCSC Ensembl
Innerchr19:23005982..23643457hg19UCSC Ensembl
Innerchr19:22797822..23435297hg18UCSC Ensembl
Innerchr19:22797822..23435297hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38637476
hg19637476
hg18637476
hg17637476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34470
Supporting Variants
SamplesNA19145
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988334
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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