A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607477



Internal ID20980548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38509596..38519327hg38UCSC Ensembl
chr7:38549196..38558927hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg389732
hg199732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156533
Samples
Known GenesAMPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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