A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014493



Internal ID21923836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38390961..38391015hg38UCSC Ensembl
chr7:38430562..38430616hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574310
Samples
Known GenesAMPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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