A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3467126



Internal ID18715458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16643671hg38UCSC Ensembl
Innerchr1:16871266..16970166hg19UCSC Ensembl
Innerchr1:16743853..16842753hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3898901
hg1998901
hg1898901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005136
Supporting Variants
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3467126
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