A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108896



Internal ID20675936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145681527..145681889hg38UCSC Ensembl
chr4:146602679..146603041hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381703
Supporting Variants
Samples
Known GenesC4orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00169


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