A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984085



Internal ID12630967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162288557..162391557hg38UCSC Ensembl
Innerchr6:162709589..162812589hg19UCSC Ensembl
Innerchr6:162629579..162732579hg18UCSC Ensembl
Innerchr6:162680000..162783000hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38103001
hg19103001
hg18103001
hg17103001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752097
Supporting Variants
SamplesBEC_768
Known GenesPARK2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984085
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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