A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435453



Internal ID21093006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136059901..136060311hg38UCSC Ensembl
chr7:135744649..135745059hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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