A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799661



Internal ID19175938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66291191..66299570hg38UCSC Ensembl
Innerchr17:64287309..64295688hg19UCSC Ensembl
Innerchr17:61717771..61726150hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg388380
hg198380
hg188380
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893035
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799661
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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