A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010667



Internal ID19099884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:100630059..100695124hg38UCSC Ensembl
Innerchr4:101551216..101616281hg19UCSC Ensembl
Innerchr4:101770239..101835304hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3865066
hg1965066
hg1865066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631009, nssv3631010
Samples
Known GenesEMCN-IT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010667
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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