A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005101



Internal ID19094318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33885014..34108692hg38UCSC Ensembl
Innerchr4:33886636..34110314hg19UCSC Ensembl
Innerchr4:33563031..33786709hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38223679
hg19223679
hg18223679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620651
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)nsv1005101
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