A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445606



Internal ID21103159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7718490..7719779hg38UCSC Ensembl
chr10:7760453..7761742hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984321
Samples
Known GenesITIH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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