A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952830



Internal ID21372900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139520461..139520536hg38UCSC Ensembl
chr7:139205207..139205282hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198396
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952830
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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