A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074427



Internal ID20641467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44044355..44074156hg38UCSC Ensembl
chr22:44440235..44470036hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3829802
hg1929802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544236
Supporting Variants
Samples
Known GenesPARVB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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