A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030484



Internal ID19119703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3325358..3466470hg38UCSC Ensembl
Innerchr7:3364990..3506102hg19UCSC Ensembl
Innerchr7:3331516..3472628hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38141113
hg19141113
hg18141113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6222n100
Supporting Variantsnssv3752790
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030484
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