A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421091



Internal ID21078644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148590908..148594127hg38UCSC Ensembl
chr7:148288000..148291219hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383220
hg193220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153963
Samples
Known GenesC7orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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