A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585226



Internal ID18883507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:12992198..13084083hg38UCSC Ensembl
Innerchr21:14364519..14456404hg19UCSC Ensembl
Innerchr21:13286390..13378275hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3891886
hg1991886
hg1891886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067370
Supporting Variants
Samples
Known GenesANKRD30BP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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