A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900981



Internal ID1450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1205865..1512249hg38UCSC Ensembl
chr2:1201551..1516021hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38306385
hg19314471
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555580
Supporting Variants
Samples
Known GenesSNTG2, TPO
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900981
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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