A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571560



Internal ID21763603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26606191..26606191hg38UCSC Ensembl
chr7:26645810..26645810hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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