A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946071



Internal ID21366141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:965203..965203hg38UCSC Ensembl
chr2:960889..960889hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186969
SamplesHG002
Known GenesSNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946071
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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