A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701751



Internal ID15438403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93019026..93025525hg38UCSC Ensembl
Innerchr7:92648340..92654839hg19UCSC Ensembl
Innerchr7:92486276..92492775hg18UCSC Ensembl
Innerchr7:92292991..92299490hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386500
hg196500
hg186500
hg176500
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525606
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701751
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