A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474176



Internal ID22532070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88454659..88460857hg38UCSC Ensembl
chr16:88521067..88527265hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg386199
hg196199
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871915
Supporting Variants
Samples
Known GenesZFPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474176
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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