A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413512



Internal ID21071065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4169901..4174700hg38UCSC Ensembl
chr6:4170135..4174934hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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