A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026684



Internal ID18769215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76514308..76818391hg38UCSC Ensembl
Innerchr7:76143625..76447708hg19UCSC Ensembl
Innerchr7:75981561..76285644hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38304084
hg19304084
hg18304084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6478n100
Supporting Variantsnssv3656555
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026684
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