A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332670



Internal ID20865844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240602101..240607500hg38UCSC Ensembl
chr1:240765401..240770800hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059546
Samples
Known GenesGREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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