A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417188



Internal ID21074741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37319007..37326701hg38UCSC Ensembl
chr8:37176525..37184219hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg387695
hg197695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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