A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515855



Internal ID15442912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6432731..6447986hg38UCSC Ensembl
Innerchr6:6432964..6448219hg19UCSC Ensembl
Innerchr6:6377963..6393218hg18UCSC Ensembl
Innerchr6:6377963..6393218hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815256
hg1915256
hg1815256
hg1715256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655157, nssv663658, nssv668686, nssv669762, nssv660850, nssv662952, nssv670723, nssv654715, nssv680177, nssv681347, nssv665025
Samples
Known GenesLY86-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515855
Frequency
Sample Size2026
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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