A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985794



Internal ID12984044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189758697..189834696hg38UCSC Ensembl
Innerchr4:190679851..190755851hg19UCSC Ensembl
Innerchr4:190916845..190992845hg18UCSC Ensembl
Innerchr4:191055000..191131000hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3876000
hg1976001
hg1876001
hg1776001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752042
Supporting Variants
SamplesSPC_50
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985794
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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