A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413929



Internal ID21071482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41352301..41353300hg38UCSC Ensembl
chr6:41320039..41321038hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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