A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380425



Internal ID21037978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67738316..67741126hg38UCSC Ensembl
chr4:68604034..68606844hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119482
Samples
Known GenesGNRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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