A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606009



Internal ID20979080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:602600..905284hg38UCSC Ensembl
chr7:642237..944921hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38302685
hg19302685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6536n223
Supporting Variantsnssv18217924
Samples
Known GenesADAP1, GET4, HEATR2, PRKAR1B, SUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer