A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370567



Internal ID22596236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56918904..56919888hg38UCSC Ensembl
chr15:57211102..57212086hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933366
Supporting Variants
Samples
Known GenesTCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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