A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627777



Internal ID21576082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75647051..75647051hg38UCSC Ensembl
chr5:74942876..74942876hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155978
SamplesHG03371
Known GenesANKDD1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627777
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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