A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949761



Internal ID21369830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97433139..97438062hg38UCSC Ensembl
chr4:98354290..98359213hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196468
SamplesHG002
Known GenesSTPG2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949761
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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