A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455463



Internal ID22513340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21549854..21552630hg38UCSC Ensembl
chr10:21838783..21841559hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382777
hg192777
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863776
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455463
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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