A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619075



Internal ID20992146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130265823..130271432hg38UCSC Ensembl
chr6:130586968..130592577hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg385610
hg195610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138447
Samples
Known GenesSAMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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