A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384125



Internal ID21041678
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 StatusM
Merged Variants
Supporting Variantsnssv18115808
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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