A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401905



Internal ID21059458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48098941..48099720hg38UCSC Ensembl
chr6:48066677..48067456hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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