A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038822



Internal ID19128041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114695888..114737445hg38UCSC Ensembl
Innerchr10:116455647..116497204hg19UCSC Ensembl
Innerchr10:116445637..116487194hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3841558
hg1941558
hg1841558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n100
Supporting Variantsnssv3510470
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)nsv1038822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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