A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828802



Internal ID22603737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19272849..19282990hg38UCSC Ensembl
chr1:19599343..19609484hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810142
hg1910142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463378
Samples
Known GenesAKR7A3, AKR7L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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