A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842214



Internal ID22617149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177149364..177154487hg38UCSC Ensembl
chr5:176576365..176581488hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg385124
hg195124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498378
Samples
Known GenesNSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842214
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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