A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600756



Internal ID20973827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108930701..108932900hg38UCSC Ensembl
chr6:109251904..109254103hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6360n223
Supporting Variantsnssv18137014
Samples
Known GenesARMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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