A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141893



Internal ID20708933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149780163..149781846hg38UCSC Ensembl
chr6:150101299..150102982hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610168
Supporting Variants
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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