A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371925



Internal ID22597594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41272673..41274210hg38UCSC Ensembl
chr15:41564871..41566408hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381538
hg191538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933461
Supporting Variants
Samples
Known GenesCHP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371925
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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