A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893006



Internal ID19183826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36804572..36849773hg38UCSC Ensembl
Outerchr17:36804572..36849773hg38UCSC Ensembl
Innerchr17:35161826..35207037hg19UCSC Ensembl
Outerchr17:35161826..35207037hg19UCSC Ensembl
Innerchr17:32235939..32281150hg18UCSC Ensembl
Outerchr17:32235939..32281150hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3845202
hg1945212
hg1845212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790753
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893006
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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