A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760635



Internal ID20536495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27107136..27107136hg38UCSC Ensembl
chr1:27433627..27433627hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381033
hg191033
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292880
Samples
Known GenesSLC9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760635
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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