A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449912



Internal ID21107465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86764552..86772811hg38UCSC Ensembl
chr10:88524309..88532568hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg388260
hg198260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984508
Samples
Known GenesBMPR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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