A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653345



Internal ID15389997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154860892..154914071hg38UCSC Ensembl
Innerchr7:154652602..154705781hg19UCSC Ensembl
Innerchr7:154283535..154336714hg18UCSC Ensembl
Innerchr7:154090250..154143429hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3853180
hg1953180
hg1853180
hg1753180
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517537
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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