A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783414



Internal ID19179735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72009977..72201879hg38UCSC Ensembl
Innerchr7:71474962..71666864hg19UCSC Ensembl
Innerchr7:71112898..71304800hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38191903
hg19191903
hg18191903
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891143
Supporting Variants
Samples
Known GenesCALN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783414
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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