A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400734



Internal ID21058287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48934288..48936720hg38UCSC Ensembl
chr6:48901925..48904357hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382433
hg192433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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