A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704151



Internal ID15094117
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527676
Supporting Variants
Samples
Known GenesTGIF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704151
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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