A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316420



Internal ID20849499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11039829..11041639hg38UCSC Ensembl
chr1:11099886..11101696hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050849
Samples
Known GenesMASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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