A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613685



Internal ID20986756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99000729..99003203hg38UCSC Ensembl
chr7:98598352..98600826hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161311
Samples
Known GenesTRRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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