A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022981



Internal ID19112198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121247848..121356060hg38UCSC Ensembl
Innerchr5:120583543..120691755hg19UCSC Ensembl
Innerchr5:120611442..120719654hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38108213
hg19108213
hg18108213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746626
Samples
Known GenesLOC102467226
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022981
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