A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014532



Internal ID20581572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87634184..87634734hg38UCSC Ensembl
chr13:88286439..88286989hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478388
Supporting Variants
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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