A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029034



Internal ID19118253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81208696..81507830hg38UCSC Ensembl
Innerchr7:80838012..81137146hg19UCSC Ensembl
Innerchr7:80675948..80975082hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38299135
hg19299135
hg18299135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755417
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)nsv1029034
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