A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048733



Internal ID18791264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112761646..112787267hg38UCSC Ensembl
Innerchr9:115523926..115549547hg19UCSC Ensembl
Innerchr9:114563747..114589368hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3825622
hg1925622
hg1825622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7702n100
Supporting Variantsnssv3695103
Samples
Known GenesSNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048733
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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