A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014077



Internal ID19103297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102313943..102347695hg38UCSC Ensembl
Innerchr3:102032787..102066539hg19UCSC Ensembl
Innerchr3:103515477..103549229hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3833753
hg1933753
hg1833753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604373
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)nsv1014077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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