A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602270



Internal ID20975341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106256717..106263077hg38UCSC Ensembl
chr6:106704592..106710952hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386361
hg196361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135358
Samples
Known GenesATG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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