A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038318



Internal ID19127537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70635513..70665972hg38UCSC Ensembl
Innerchr10:72395269..72425728hg19UCSC Ensembl
Innerchr10:72065275..72095734hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3830460
hg1930460
hg1830460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv923n100
Supporting Variantsnssv3508446
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)nsv1038318
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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