A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431838



Internal ID21089391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141892301..141893200hg38UCSC Ensembl
chr7:141592101..141593000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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