A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613963



Internal ID20987034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24709510..24709900hg38UCSC Ensembl
chr7:24749129..24749519hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233080
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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