A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695848



Internal ID15432500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152515952..152525209hg38UCSC Ensembl
Innerchr1:152488428..152497685hg19UCSC Ensembl
Innerchr1:150755052..150764309hg18UCSC Ensembl
Innerchr1:149301501..149310758hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389258
hg199258
hg189258
hg179258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518413
Supporting Variants
Samples
Known GenesCRCT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695848
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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