A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985121



Internal ID20552161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86854101..86861200hg38UCSC Ensembl
chr10:88613858..88620957hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449372
Supporting Variants
Samples
Known GenesBMPR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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