A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453617



Internal ID21111170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79536191..79575518hg38UCSC Ensembl
chr10:81295947..81335274hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3839328
hg1939328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983600
Samples
Known GenesSFTPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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