A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701814



Internal ID15091780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18288214..19009043hg38UCSC Ensembl
Innerchr9:18288212..19009041hg19UCSC Ensembl
Innerchr9:18278212..18999041hg18UCSC Ensembl
Innerchr9:18278212..18999041hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38720830
hg19720830
hg18720830
hg17720830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525659
Supporting Variants
Samples
Known GenesADAMTSL1, FAM154A, MIR3152
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701814
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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