A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358849



Internal ID22584518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211953441..211953560hg38UCSC Ensembl
chr1:212126783..212126902hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868746
Supporting Variants
Samples
Known GenesINTS7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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