A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036470



Internal ID18779001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77448138..77471048hg38UCSC Ensembl
Innerchr9:80063054..80085964hg19UCSC Ensembl
Innerchr9:79252874..79275784hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3822911
hg1922911
hg1822911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759776
Samples
Known GenesGNA14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036470
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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