A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889012



Internal ID22664023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38817016..38827403hg38UCSC Ensembl
chr6:38784792..38795179hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3810388
hg1910388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446607
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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