A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518773



Internal ID15099380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149188785..149225575hg38UCSC Ensembl
Innerchr7:148885877..148922666hg19UCSC Ensembl
Innerchr7:148516810..148553599hg18UCSC Ensembl
Innerchr7:148323525..148360314hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3836791
hg1936790
hg1836790
hg1736790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696224
Samples
Known GenesZNF282
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518773
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