A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905038



Internal ID22680219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87716551..87719633hg38UCSC Ensembl
chr6:88426269..88429351hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383083
hg193083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905038
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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