A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617352



Internal ID20990423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99965486..99978800hg38UCSC Ensembl
chr6:100413362..100426676hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3813315
hg1913315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147669
Samples
Known GenesMCHR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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