A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427162



Internal ID22485032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150931979..150932586hg38UCSC Ensembl
chr6:151253115..151253722hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903930
Supporting Variants
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427162
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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