A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789074



Internal ID18822254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143719827..143760627hg38UCSC Ensembl
Innerchr7:143416920..143457720hg19UCSC Ensembl
Innerchr7:143047853..143088653hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3840801
hg1940801
hg1840801
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891222
Supporting Variants
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789074
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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