A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115808



Internal ID20682848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175746850..175755292hg38UCSC Ensembl
chr4:176668001..176676443hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg388443
hg198443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384125
Supporting Variants
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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