A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527256



Internal ID15107863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175461719..175613114hg38UCSC Ensembl
Innerchr1:175430855..175582250hg19UCSC Ensembl
Innerchr1:173697478..173848873hg18UCSC Ensembl
Innerchr1:172162512..172313907hg17UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38151396
hg19151396
hg18151396
hg17151396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703660
Samples
Known GenesTNR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527256
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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