A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615029



Internal ID20988100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101036601..101039400hg38UCSC Ensembl
chr6:101484477..101487276hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6340n223
Supporting Variantsnssv18133840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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