A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013937



Internal ID19103156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:242586425..242691129hg38UCSC Ensembl
Innerchr1:242749727..242854431hg19UCSC Ensembl
Innerchr1:240816350..240921054hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38104705
hg19104705
hg18104705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496131
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)nsv1013937
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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