A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698792



Internal ID18650387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16518425..16627335hg38UCSC Ensembl
Innerchr1:16844920..16953830hg19UCSC Ensembl
Innerchr1:16717507..16826417hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38108911
hg19108911
hg18108911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009058
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)nssv3698792
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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