A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526367



Internal ID15106974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103477009..103787255hg38UCSC Ensembl
Innerchr1:104019631..104329877hg19UCSC Ensembl
Innerchr1:103792219..104131400hg18UCSC Ensembl
Innerchr1:103731652..104041898hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38310247
hg19310247
hg18339182
hg17310247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702661
Samples
Known GenesACTG1P4, AMY1A, AMY1B, AMY1C, AMY2A, AMY2B, LOC101928436, RNPC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526367
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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