A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979102



Internal ID12632945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36643835..36835382hg38UCSC Ensembl
Innerchr19:37134737..37326284hg19UCSC Ensembl
Innerchr19:41826577..42018124hg18UCSC Ensembl
Innerchr19:41826577..42018124hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38191548
hg19191548
hg18191548
hg17191548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34384
Supporting Variants
SamplesNA12891
Known GenesZNF461, ZNF567, ZNF790, ZNF790-AS1, ZNF850
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979102
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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