A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537321



Internal ID21861676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54504649..54752462hg38UCSC Ensembl
chr1:54970322..55218135hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38247814
hg19247814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984389
Supporting Variants
Samples
Known GenesACOT11, FAM151A, MROH7, MROH7-TTC4, TTC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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