A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384468



Internal ID22442338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32731795..32731887hg38UCSC Ensembl
chr15:33023996..33024088hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928498
Supporting Variants
Samples
Known GenesGREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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