A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893002



Internal ID19183822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36102943..36139251hg38UCSC Ensembl
Outerchr17:36102943..36139251hg38UCSC Ensembl
Innerchr17:34430336..34466631hg19UCSC Ensembl
Outerchr17:34430336..34466631hg19UCSC Ensembl
Innerchr17:31454449..31490744hg18UCSC Ensembl
Outerchr17:31454449..31490744hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3836309
hg1936296
hg1836296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779519, essv25800961
Samples
Known GenesCCL4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893002
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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