A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799961



Internal ID18830109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40263685..40320658hg38UCSC Ensembl
Innerchr7:40303284..40360257hg19UCSC Ensembl
Innerchr7:40269809..40326782hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3856974
hg1956974
hg1856974
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891101
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799961
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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