A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438156



Internal ID21095709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33906801..33914500hg38UCSC Ensembl
chr10:34195729..34203428hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv677n223
Supporting Variantsnssv17979794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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