A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405451



Internal ID21063004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35906325..35906538hg38UCSC Ensembl
chr6:35874102..35874315hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141734
Samples
Known GenesSRPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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