A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618882



Internal ID20991953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43974415..43976584hg38UCSC Ensembl
chr7:44014014..44016183hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154586
Samples
Known GenesPOLR2J4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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