A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394600



Internal ID21052153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175706736..175910116hg38UCSC Ensembl
chr4:176627887..176831267hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38203381
hg19203381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212778
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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