A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604625



Internal ID20977696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45862301..45870800hg38UCSC Ensembl
chr7:45901900..45910399hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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