A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052912



Internal ID19142131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91083796..91104080hg38UCSC Ensembl
Innerchr9:93846078..93866362hg19UCSC Ensembl
Innerchr9:92885899..92906183hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3820285
hg1920285
hg1820285
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697547, nssv3697548
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052912
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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