A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614663



Internal ID20987734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29628701..29659200hg38UCSC Ensembl
chr7:29668317..29698816hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6632n223
Supporting Variantsnssv18228998
Samples
Known GenesLOC646762
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614663
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