A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601284



Internal ID20974355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126668840..126742393hg38UCSC Ensembl
chr6:126989986..127063538hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3873554
hg1973553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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