A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436182



Internal ID21093735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119209805..119214006hg38UCSC Ensembl
chr10:120969317..120973518hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384202
hg194202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979603
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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