A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579936



Internal ID18878217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97051523..97545714hg38UCSC Ensembl
Innerchr2:97717260..98162177hg19UCSC Ensembl
Innerchr2:97080987..97528609hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38494192
hg19444918
hg18447623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009571
Supporting Variants
Samples
Known GenesANKRD36, ANKRD36B, FAHD2B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579936
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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