A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704108



Internal ID21376384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437675..37438001hg38UCSC Ensembl
chr7:37477278..37477604hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392912
Supporting Variants
Samples
Known GenesELMO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704108
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.666667


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