A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606962



Internal ID20980033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43996005..43998327hg38UCSC Ensembl
chr7:44035604..44037926hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382323
hg192323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154590
Samples
Known GenesPOLR2J4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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