A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527676



Internal ID15108283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3445828..3452980hg38UCSC Ensembl
Innerchr18:3445826..3452978hg19UCSC Ensembl
Innerchr18:3435826..3442978hg18UCSC Ensembl
Innerchr18:3435826..3442978hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387153
hg197153
hg187153
hg177153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704151
Samples
Known GenesTGIF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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