A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401671



Internal ID21059224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92860901..92896600hg38UCSC Ensembl
chr6:93570619..93606318hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3835700
hg1935700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6313n223
Supporting Variantsnssv18237029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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