A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980792



Internal ID12625301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161849949..161893522hg38UCSC Ensembl
Innerchr6:162270981..162314554hg19UCSC Ensembl
Innerchr6:162190971..162234544hg18UCSC Ensembl
Innerchr6:162241392..162284965hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3843574
hg1943574
hg1843574
hg1743574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752092
Supporting Variants
SamplesBEC_158
Known GenesPARK2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980792
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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