A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985174



Internal ID12982903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60103634..60278031hg38UCSC Ensembl
Innerchr3:60089360..60263760hg19UCSC Ensembl
Innerchr3:60064400..60238800hg18UCSC Ensembl
Innerchr3:60064400..60238800hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38174398
hg19174401
hg18174401
hg17174401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752010
Supporting Variants
SamplesSPC_113
Known GenesFHIT
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985174
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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