A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426381



Internal ID21083934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130734621..130734692hg38UCSC Ensembl
chr7:130419382..130419453hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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