A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039035



Internal ID19128254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126181994..126220371hg38UCSC Ensembl
Innerchr9:128944273..128982650hg19UCSC Ensembl
Innerchr9:127984094..128022471hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7717n100
Supporting Variantsnssv3695242
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)nsv1039035
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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