A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028776



Internal ID18771307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80785320..80925968hg38UCSC Ensembl
Innerchr7:80414636..80555284hg19UCSC Ensembl
Innerchr7:80252572..80393220hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38140649
hg19140649
hg18140649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655144, nssv3655143
Samples
Known GenesSEMA3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028776
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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