A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893035



Internal ID19183855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66291191..66299570hg38UCSC Ensembl
Outerchr17:66291191..66299570hg38UCSC Ensembl
Innerchr17:64287309..64295688hg19UCSC Ensembl
Outerchr17:64287309..64295688hg19UCSC Ensembl
Innerchr17:61717771..61726150hg18UCSC Ensembl
Outerchr17:61717771..61726150hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg388380
hg198380
hg188380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779000, essv25779391, essv25799661, essv25778906, essv25787029, essv25787432, essv25787005
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893035
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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