A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851405



Internal ID22626340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143105098..143110426hg38UCSC Ensembl
chr7:142802191..142807519hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385329
hg195329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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