A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329481



Internal ID20862633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24363188..24376722hg38UCSC Ensembl
chr1:24689678..24703212hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3813535
hg1913535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059577
Samples
Known GenesGRHL3, STPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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