A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663700



Internal ID15053666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3448764..3451764hg38UCSC Ensembl
Innerchr18:3448762..3451762hg19UCSC Ensembl
Innerchr18:3438762..3441762hg18UCSC Ensembl
Innerchr18:3438762..3441762hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383001
hg193001
hg183001
hg173001
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516490
Supporting Variants
Samples
Known GenesTGIF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663700
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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