A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410655



Internal ID21068208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36102342..36102416hg38UCSC Ensembl
chr6:36070119..36070193hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141735
Samples
Known GenesMAPK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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