A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425321



Internal ID21082874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139958829..139963049hg38UCSC Ensembl
chr7:139658628..139662848hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384221
hg194221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155301
Samples
Known GenesTBXAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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