A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422690



Internal ID21080243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145994044..145999612hg38UCSC Ensembl
chr7:145691137..145696705hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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