A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074251



Internal ID21983484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32581257..32581257hg38UCSC Ensembl
chr7:32620869..32620869hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569448
Samples
Known GenesAVL9, DPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074251
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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