A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442556



Internal ID22500426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49982274..49990283hg38UCSC Ensembl
chr6:49949987..49957996hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg388010
hg198010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442556
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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