A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892496



Internal ID22667548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144224080..144235171hg38UCSC Ensembl
chr6:144545217..144556307hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3811092
hg1911091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892496
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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