A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044989



Internal ID19134208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70352677..70394751hg38UCSC Ensembl
Innerchr10:72112433..72154507hg19UCSC Ensembl
Innerchr10:71782439..71824513hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3842075
hg1942075
hg1842075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv922n100
Supporting Variantsnssv3511497
Samples
Known GenesLRRC20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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