A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051194



Internal ID19140413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91608755..91631952hg38UCSC Ensembl
Innerchr9:94371037..94394234hg19UCSC Ensembl
Innerchr9:93410858..93434055hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3823198
hg1923198
hg1823198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697550
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)nsv1051194
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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