A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833997



Internal ID22608932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62130570..62148727hg38UCSC Ensembl
chr2:62357705..62375862hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3818158
hg1918158
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487561
Samples
Known GenesCOMMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833997
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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