A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670899



Internal ID15407551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113012888..113053118hg38UCSC Ensembl
Innerchr9:115775168..115815398hg19UCSC Ensembl
Innerchr9:114814989..114855219hg18UCSC Ensembl
Innerchr9:112854723..112894953hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3840231
hg1940231
hg1840231
hg1740231
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)nssv670899
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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