A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602765



Internal ID20975836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99963901..99964842hg38UCSC Ensembl
chr6:100411777..100412718hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147668
Samples
Known GenesMCHR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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