A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335557



Internal ID20868750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:255382..256480hg38UCSC Ensembl
chr2:255382..256480hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085612
Samples
Known GenesSH3YL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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