A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507769



Internal ID20881064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64705401..64716500hg38UCSC Ensembl
chr15:64997600..65008699hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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