A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890740



Internal ID22665769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35842225..35842337hg38UCSC Ensembl
chr6:35810002..35810114hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440699
Samples
Known GenesSRPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890740
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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