A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425234



Internal ID21082787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130155315..130157211hg38UCSC Ensembl
chr7:129795155..129797051hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381897
hg191897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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