A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701574



Internal ID15091540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23369659..23374819hg38UCSC Ensembl
Innerchr1:23696152..23701312hg19UCSC Ensembl
Innerchr1:23568739..23573899hg18UCSC Ensembl
Innerchr1:23441458..23446618hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg385161
hg195161
hg185161
hg175161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525446
Supporting Variants
Samples
Known GenesC1orf213, ZNF436
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701574
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