A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525319



Internal ID15452612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128289218..128306120hg38UCSC Ensembl
Innerchr7:127929271..127946173hg19UCSC Ensembl
Innerchr7:127716507..127733409hg18UCSC Ensembl
Innerchr7:127523222..127540124hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3816903
hg1916903
hg1816903
hg1716903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701428
Samples
Known GenesMGC27345
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525319
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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