A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026461



Internal ID19115679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5852346..5931291hg38UCSC Ensembl
Innerchr7:5891977..5970922hg19UCSC Ensembl
Innerchr7:5858503..5937448hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3878946
hg1978946
hg1878946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6243n100
Supporting Variantsnssv3655070
Samples
Known GenesCCZ1, OCM, RSPH10B, RSPH10B2, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026461
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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