A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051372



Internal ID19140591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119729312..119767916hg38UCSC Ensembl
Innerchr9:122491590..122530194hg19UCSC Ensembl
Innerchr9:121531411..121570015hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3838605
hg1938605
hg1838605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7713n100
Supporting Variantsnssv3759822
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)nsv1051372
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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