A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618389



Internal ID20991460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25152329..25154247hg38UCSC Ensembl
chr7:25191948..25193866hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155521
Samples
Known GenesC7orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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