A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428708



Internal ID207568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156017511..156017911hg38UCSC Ensembl
chr1:155987302..155987702hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891261
Samples
Known GenesSSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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