A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978022



Internal ID12631807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167885235..168058165hg38UCSC Ensembl
Innerchr4:168806386..168979316hg19UCSC Ensembl
Innerchr4:169042961..169215891hg18UCSC Ensembl
Innerchr4:169181116..169354046hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38172931
hg19172931
hg18172931
hg17172931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35159
Supporting Variants
SamplesNA10857
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978022
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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