A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766778



Internal ID22101176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2884197..2884272hg38UCSC Ensembl
chr2:2887969..2888044hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4439467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766778
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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