A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799902



Internal ID18834116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162346650..162372992hg38UCSC Ensembl
Innerchr6:162767682..162794024hg19UCSC Ensembl
Innerchr6:162687672..162714014hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826343
hg1926343
hg1826343
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890988
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799902
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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