A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046888



Internal ID19136107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114695284..114745881hg38UCSC Ensembl
Innerchr10:116455043..116505640hg19UCSC Ensembl
Innerchr10:116445033..116495630hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3850598
hg1950598
hg1850598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n100
Supporting Variantsnssv3509351
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)nsv1046888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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