A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987829



Internal ID12625078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167893121..168058165hg38UCSC Ensembl
Innerchr4:168814272..168979316hg19UCSC Ensembl
Innerchr4:169050847..169215891hg18UCSC Ensembl
Innerchr4:169189002..169354046hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38165045
hg19165045
hg18165045
hg17165045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752039
Supporting Variants
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987829
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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