A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323236



Internal ID20856353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150644269..150652055hg38UCSC Ensembl
chr1:150616745..150624531hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387787
hg197787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052982
Samples
Known GenesGOLPH3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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