A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023288



Internal ID19112505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4592601..4624890hg38UCSC Ensembl
Innerchr9:4592601..4624890hg19UCSC Ensembl
Innerchr9:4582601..4614890hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3832290
hg1932290
hg1832290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692393
Samples
Known GenesSPATA6L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023288
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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