A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673709



Internal ID15063675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46911729..46967279hg38UCSC Ensembl
Innerchr19:47414986..47470536hg19UCSC Ensembl
Innerchr19:52106826..52162376hg18UCSC Ensembl
Innerchr19:52106826..52162376hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3855551
hg1955551
hg1855551
hg1755551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520664
Supporting Variants
Samples
Known GenesARHGAP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673709
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