A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427429



Internal ID21084982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140255525..140256876hg38UCSC Ensembl
chr7:139955325..139956676hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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