A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423273



Internal ID22481143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154991201..154993037hg38UCSC Ensembl
chr6:155312335..155314171hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423273
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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