A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853260



Internal ID22628195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37199726..37205277hg38UCSC Ensembl
chr9:37199723..37205274hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg385552
hg195552
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513044
Samples
Known GenesZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853260
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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