A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932966



Internal ID21353035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75712132..75712292hg38UCSC Ensembl
chr2:75939258..75939418hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177063
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932966
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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