A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114341



Internal ID20681381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177897701..178198500hg38UCSC Ensembl
chr4:178818855..179119654hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38300800
hg19300800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376563
Supporting Variants
Samples
Known GenesLINC01098, LINC01099
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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