A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014510



Internal ID19103728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218802419..219018616hg38UCSC Ensembl
Innerchr1:218975761..219191958hg19UCSC Ensembl
Innerchr1:217042384..217258581hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38216198
hg19216198
hg18216198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3497742
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)nsv1014510
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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