A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434268



Internal ID21091821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128478401..128484800hg38UCSC Ensembl
chr7:128118455..128124854hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153306
Samples
Known GenesMETTL2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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