A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656909



Internal ID15046875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226187566..226301125hg38UCSC Ensembl
Innerchr1:226375267..226488826hg19UCSC Ensembl
Innerchr1:224441890..224555449hg18UCSC Ensembl
Innerchr1:222682002..222795561hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38113560
hg19113560
hg18113560
hg17113560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517107
Supporting Variants
Samples
Known GenesLIN9, MIXL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656909
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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