A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018703



Internal ID19107920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64945771hg38UCSC Ensembl
Innerchr9:69695973..69958189hg19UCSC Ensembl
Innerchr9:68985793..69248009hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38262217
hg19262217
hg18262217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n100
Supporting Variantsnssv3759742, nssv3696164, nssv3696165
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)nsv1018703
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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