A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985435



Internal ID12635597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22823158..23460658hg38UCSC Ensembl
Innerchr19:23005960..23643460hg19UCSC Ensembl
Innerchr19:22797800..23435300hg18UCSC Ensembl
Innerchr19:22797800..23435300hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38637501
hg19637501
hg18637501
hg17637501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34907
Supporting Variants
SamplesNA19144
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)essv6985435
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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