A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442819



Internal ID22500689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37639111..37639167hg38UCSC Ensembl
chr6:37606887..37606943hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894405
Supporting Variants
Samples
Known GenesMDGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442819
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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