A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617039



Internal ID20990110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151850389..151856797hg38UCSC Ensembl
chr6:152171524..152177932hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386409
hg196409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141519
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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