A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767568



Internal ID22102050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160089655..160089784hg38UCSC Ensembl
chr2:160946166..160946295hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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