A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830546



Internal ID22605481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:935164..964006hg38UCSC Ensembl
chr1:870544..899386hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3828843
hg1928843
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482485
Samples
Known GenesKLHL17, NOC2L, SAMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830546
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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