A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518903



Internal ID15446196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7452965..7458638hg38UCSC Ensembl
Innerchr1:7513025..7518698hg19UCSC Ensembl
Innerchr1:7435612..7441285hg18UCSC Ensembl
Innerchr1:7447291..7452964hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg385674
hg195674
hg185674
hg175674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696361
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518903
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