A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654199



Internal ID15390851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113012888..113052193hg38UCSC Ensembl
Innerchr9:115775168..115814473hg19UCSC Ensembl
Innerchr9:114814989..114854294hg18UCSC Ensembl
Innerchr9:112854723..112894028hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3839306
hg1939306
hg1839306
hg1739306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517282
Supporting Variants
Samples
Known GenesZFP37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654199
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