A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418978



Internal ID21076531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141487504..141487945hg38UCSC Ensembl
chr7:141187304..141187745hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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