A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576935



Internal ID18875216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:6487675..6506444hg38UCSC Ensembl
Innerchr2:6627807..6646576hg19UCSC Ensembl
Innerchr2:6545258..6564027hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3818770
hg1918770
hg1818770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000891
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576935
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