A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987729



Internal ID12981382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104385032..105055460hg38UCSC Ensembl
Innerchr3:104103876..104774304hg19UCSC Ensembl
Innerchr3:105586566..106256994hg18UCSC Ensembl
Innerchr3:105586566..106256994hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38670429
hg19670429
hg18670429
hg17670429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35023
Supporting Variants
SamplesNA18966
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987729
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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