A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042549



Internal ID19131768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44576442..44622018hg38UCSC Ensembl
Innerchr10:45071890..45117466hg19UCSC Ensembl
Innerchr10:44391896..44437472hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3845577
hg1945577
hg1845577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511218
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)nsv1042549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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