A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049708



Internal ID19138927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19030782..19058141hg38UCSC Ensembl
Innerchr10:19319711..19347070hg19UCSC Ensembl
Innerchr10:19359717..19387076hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3827360
hg1927360
hg1827360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv682n100
Supporting Variantsnssv3509320, nssv3522591, nssv3516988, nssv3518120, nssv3509521, nssv3505775
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)nsv1049708
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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