A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001936



Internal ID19091153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22494218..22521753hg38UCSC Ensembl
Innerchr2:22717090..22744625hg19UCSC Ensembl
Innerchr2:22570595..22598130hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3827536
hg1927536
hg1827536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579012
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)nsv1001936
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