A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615821



Internal ID20988892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156686201..156688500hg38UCSC Ensembl
chr6:157007335..157009634hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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