A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784543



Internal ID19166665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34065327..34072955hg38UCSC Ensembl
Innerchr17:32392346..32399974hg19UCSC Ensembl
Innerchr17:29416459..29424087hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387629
hg197629
hg187629
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892996
Supporting Variants
Samples
Known GenesASIC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784543
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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