A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117561



Internal ID20684601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44681827..44682386hg38UCSC Ensembl
chr4:44683844..44684403hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393707
Supporting Variants
Samples
Known GenesGUF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00099


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