A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612193



Internal ID20985264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118056089..118062837hg38UCSC Ensembl
chr7:117696143..117702891hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg386749
hg196749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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