A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3753034



Internal ID18704629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62722439..63818912hg38UCSC Ensembl
Innerchr7:62182817..63279290hg19UCSC Ensembl
Innerchr7:61820252..62916725hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381096474
hg191096474
hg181096474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033831
Supporting Variants
Samples
Known GenesLOC100287704, LOC100287834, MIR4283-1, MIR4283-2, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3753034
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