A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434725



Internal ID22492595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39710094..39710094hg38UCSC Ensembl
chr7:39749693..39749693hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434725
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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