A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705727



Internal ID15095693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75312355..75787707hg38UCSC Ensembl
Innerchr3:75361506..75836858hg19UCSC Ensembl
Innerchr3:75444196..75919548hg18UCSC Ensembl
Innerchr3:75444196..75919548hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38475353
hg19475353
hg18475353
hg17475353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529016
Supporting Variants
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705727
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