A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418824



Internal ID21076377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129195984..129196868hg38UCSC Ensembl
chr7:128835825..128836709hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153342
Samples
Known GenesSMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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