A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420237



Internal ID22478107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103708910..103734284hg38UCSC Ensembl
chr6:104156785..104182159hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3825375
hg1925375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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