A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048835



Internal ID19138054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81085989..81150852hg38UCSC Ensembl
Innerchr9:83700904..83765767hg19UCSC Ensembl
Innerchr9:82890724..82955587hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3864864
hg1964864
hg1864864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697519
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)nsv1048835
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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