A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013943



Internal ID19103162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:222297558..222322146hg38UCSC Ensembl
Innerchr1:222470900..222495488hg19UCSC Ensembl
Innerchr1:220537523..220562111hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3824589
hg1924589
hg1824589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482803, nssv3501274
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)nsv1013943
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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