A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604783



Internal ID20977854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100964672..100965013hg38UCSC Ensembl
chr6:101412548..101412889hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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