A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987931



Internal ID12973054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7044026..7159629hg38UCSC Ensembl
Innerchr3:7085713..7201316hg19UCSC Ensembl
Innerchr3:7060713..7176316hg18UCSC Ensembl
Innerchr3:7060713..7176316hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38115604
hg19115604
hg18115604
hg17115604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752015
Supporting Variants
SamplesBEC_374
Known GenesGRM7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987931
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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