A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947832



Internal ID21367901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437674..37438001hg38UCSC Ensembl
chr7:37477277..37477604hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198574
SamplesHG002
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947832
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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