A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979101



Internal ID12632944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36643166..36839711hg38UCSC Ensembl
Innerchr19:37134068..37330613hg19UCSC Ensembl
Innerchr19:41825908..42022453hg18UCSC Ensembl
Innerchr19:41825908..42022453hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38196546
hg19196546
hg18196546
hg17196546
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979101
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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