A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695438



Internal ID15085404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75539242..75825134hg38UCSC Ensembl
Innerchr7:75168562..75454452hg19UCSC Ensembl
Innerchr7:75006498..75292388hg18UCSC Ensembl
Innerchr7:74813213..75099103hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38285893
hg19285891
hg18285891
hg17285891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518028
Supporting Variants
Samples
Known GenesCCL24, CCL26, HIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695438
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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