A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443863



Internal ID21101416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50535709..50536980hg38UCSC Ensembl
chr10:52295469..52296740hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981885
Samples
Known GenesSGMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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