A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829599



Internal ID22604534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:246943163..246947609hg38UCSC Ensembl
chr1:247106465..247110911hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg384447
hg194447
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463016
Samples
Known GenesZNF670-ZNF695, ZNF695
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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