A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679636



Internal ID15069602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226235871..226301125hg38UCSC Ensembl
Innerchr1:226423572..226488826hg19UCSC Ensembl
Innerchr1:224490195..224555449hg18UCSC Ensembl
Innerchr1:222730307..222795561hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3865255
hg1965255
hg1865255
hg1765255
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517107
Supporting Variants
Samples
Known GenesLIN9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679636
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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