A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518027



Internal ID15098634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2603973..2714033hg38UCSC Ensembl
Innerchr7:2643607..2753667hg19UCSC Ensembl
Innerchr7:2610133..2720193hg18UCSC Ensembl
Innerchr7:2416848..2526908hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38110061
hg19110061
hg18110061
hg17110061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv401n21
Supporting Variantsnssv695437
Samples
Known GenesAMZ1, IQCE, TTYH3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518027
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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