A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616699



Internal ID20989770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24759751..24762847hg38UCSC Ensembl
chr7:24799370..24802466hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383097
hg193097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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