A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555448



Internal ID328604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203948268..203948291hg38UCSC Ensembl
chr2:204812991..204813014hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3824
hg1924
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924690
Samples
Known GenesICOS
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555448
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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