A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351295



Internal ID21008848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171165766..171166073hg38UCSC Ensembl
chr2:172022276..172022583hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080368
Samples
Known GenesTLK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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