A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468256



Internal ID22526145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121213129..121224083hg38UCSC Ensembl
chr12:121650932..121661886hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3810955
hg1910955
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850370
Supporting Variants
Samples
Known GenesP2RX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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