A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791011



Internal ID19172321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54059004..54116368hg38UCSC Ensembl
Innerchr7:54126697..54184061hg19UCSC Ensembl
Innerchr7:54094191..54151555hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3857365
hg1957365
hg1857365
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891112
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791011
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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