A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031549



Internal ID19120771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104170839..104198413hg38UCSC Ensembl
Innerchr5:103506540..103534114hg19UCSC Ensembl
Innerchr5:103534439..103562013hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3827575
hg1927575
hg1827575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5753n100
Supporting Variantsnssv3645916
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)nsv1031549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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