A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766877



Internal ID22101351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42021918..42022102hg38UCSC Ensembl
chr4:42023935..42024119hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437447
Supporting Variants
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766877
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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