A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037888



Internal ID19127107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126236970..126272730hg38UCSC Ensembl
Innerchr9:128999249..129035009hg19UCSC Ensembl
Innerchr9:128039070..128074830hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3835761
hg1935761
hg1835761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695247
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)nsv1037888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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