A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419073



Internal ID21076626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149156596..149157272hg38UCSC Ensembl
chr7:148853688..148854364hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154015
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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