A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046998



Internal ID19136217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19684167..19742539hg38UCSC Ensembl
Innerchr10:19973096..20031468hg19UCSC Ensembl
Innerchr10:20013102..20071474hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3858373
hg1958373
hg1858373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516773
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)nsv1046998
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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