A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980929



Internal ID12635614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22739747..23476656hg38UCSC Ensembl
Innerchr19:22922549..23659458hg19UCSC Ensembl
Innerchr19:22714389..23451298hg18UCSC Ensembl
Innerchr19:22714389..23451298hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38736910
hg19736910
hg18736910
hg17736910
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, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980929
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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