A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605649



Internal ID20978720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139980501..139983200hg38UCSC Ensembl
chr6:140301638..140304337hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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