A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608435



Internal ID20981506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94228224..94228823hg38UCSC Ensembl
chr7:93857536..93858135hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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