A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626237



Internal ID21574542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36934502..36934502hg38UCSC Ensembl
chr7:36974107..36974107hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg384759
hg194759
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156970
SamplesHG02818
Known GenesELMO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626237
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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