A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429653



Internal ID22487523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84047908..84055323hg38UCSC Ensembl
chr6:84757627..84765042hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg387416
hg197416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904395
Supporting Variants
Samples
Known GenesMRAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429653
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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