A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028503



Internal ID19117721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87055198..87148731hg38UCSC Ensembl
Innerchr7:86684514..86778047hg19UCSC Ensembl
Innerchr7:86522450..86615983hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3893534
hg1993534
hg1893534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655185
Samples
Known GenesKIAA1324L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028503
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