A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872978



Internal ID22647920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72060816..72076890hg38UCSC Ensembl
chr16:72094715..72110789hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3816075
hg1916075
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472748, nssv17472747, nssv17472746, nssv17472745, nssv17472749, nssv17479099
Samples
Known GenesHP, HPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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