A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619785



Internal ID20992856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150936714..150937332hg38UCSC Ensembl
chr6:151257850..151258468hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141057
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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