A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610860



Internal ID20983931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119287219..119287725hg38UCSC Ensembl
chr6:119608384..119608890hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138833
Samples
Known GenesMAN1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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