A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027387



Internal ID20594427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90726525..90728580hg38UCSC Ensembl
chr15:91269756..91271811hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382056
hg192056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509814
Supporting Variants
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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