A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021101



Internal ID18763635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91292598..92113836hg38UCSC Ensembl
Innerchr7:90921913..91743150hg19UCSC Ensembl
Innerchr7:90759849..91581086hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38821239
hg19821238
hg18821238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755435
Samples
Known GenesAKAP9, CYP51A1, MTERF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021101
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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