A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602354



Internal ID20975425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55648151..55653454hg38UCSC Ensembl
chr7:55715844..55721147hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg385304
hg195304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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