A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009268



Internal ID18751799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59522146..59592595hg38UCSC Ensembl
Innerchr1:59987818..60058267hg19UCSC Ensembl
Innerchr1:59760406..59830855hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3870450
hg1970450
hg1870450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3467394
Samples
Known GenesFGGY
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009268
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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