A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696760



Internal ID18648355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3730448..3791316hg38UCSC Ensembl
Innerchr1:3647012..3707880hg19UCSC Ensembl
Innerchr1:3636872..3697740hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3860869
hg1960869
hg1860869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002837
Supporting Variants
Samples
Known GenesCCDC27, LRRC47, SMIM1, TP73, TP73-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696760
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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