A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422801



Internal ID22480671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113621725..113621808hg38UCSC Ensembl
chr6:113942927..113943010hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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