A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435921



Internal ID22493791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38752113..38752345hg38UCSC Ensembl
chr6:38719889..38720121hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906774
Supporting Variants
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435921
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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