A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436149



Internal ID21093702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127172560..127260856hg38UCSC Ensembl
chr10:128970824..129059120hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3888297
hg1988297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978394
Samples
Known GenesDOCK1, FAM196A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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