A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581593



Internal ID18879874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44417118..44452146hg38UCSC Ensembl
Innerchr2:44644257..44679285hg19UCSC Ensembl
Innerchr2:44497761..44532789hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3835029
hg1935029
hg1835029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006079
Supporting Variants
Samples
Known GenesCAMKMT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3581593
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