A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907348



Internal ID22682555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34251107..34252065hg38UCSC Ensembl
chr6:34218884..34219842hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38959
hg19959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907348
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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