A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437530



Internal ID21095083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103789966..103793275hg38UCSC Ensembl
chr10:105549724..105553033hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383310
hg193310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977714
Samples
Known GenesSH3PXD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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