A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117574



Internal ID20684614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44771572..44772156hg38UCSC Ensembl
chr4:44773589..44774173hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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