A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422892



Internal ID21080445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135678137..135679900hg38UCSC Ensembl
chr7:135362885..135364648hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381764
hg191764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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