A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401026



Internal ID21058579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35850109..35850405hg38UCSC Ensembl
chr6:35817886..35818182hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141730
Samples
Known GenesSRPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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