A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440759



Internal ID21098312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127020366..127154859hg38UCSC Ensembl
chr10:128818630..128953123hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38134494
hg19134494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978385
Samples
Known GenesDOCK1, FAM196A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer