A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404605



Internal ID22462475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72087726..72087826hg38UCSC Ensembl
chr2:72314856..72314956hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404605
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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