A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561897



Internal ID334864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211769397..211775177hg38UCSC Ensembl
chr2:212634122..212639902hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg385781
hg195781
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924525
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561897
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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