A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978112



Internal ID12631969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22589858..22696458hg38UCSC Ensembl
Innerchr19:22772660..22879260hg19UCSC Ensembl
Innerchr19:22564500..22671100hg18UCSC Ensembl
Innerchr19:22564500..22671100hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38106601
hg19106601
hg18106601
hg17106601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34340
Supporting Variants
SamplesNA11839
Known GenesLOC100996349, LOC440518, ZNF492
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978112
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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