A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989241



Internal ID12625480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138021905..138171908hg38UCSC Ensembl
Innerchr3:137740747..137890750hg19UCSC Ensembl
Innerchr3:139223437..139373440hg18UCSC Ensembl
Innerchr3:139223445..139373448hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38150004
hg19150004
hg18150004
hg17150004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751978
Supporting Variants
SamplesBEC_236
Known GenesA4GNT, CLDN18, DBR1, DZIP1L
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989241
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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