A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361883



Internal ID22587552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31975212..31975993hg38UCSC Ensembl
chr12:32128146..32128927hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927256
Supporting Variants
Samples
Known GenesKIAA1551
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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