A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405455



Internal ID21063008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75639301..75640000hg38UCSC Ensembl
chr6:76349017..76349716hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145213
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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