A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429799



Internal ID22487669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88122429..88128440hg38UCSC Ensembl
chr6:88832148..88838159hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg386012
hg196012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429799
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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