A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502428



Internal ID22560368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150996209..151015231hg38UCSC Ensembl
chr6:151317345..151336367hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819023
hg1919023
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844083
Supporting Variants
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502428
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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