A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043534



Internal ID19132753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56570760..56721030hg38UCSC Ensembl
Innerchr10:58330520..58480790hg19UCSC Ensembl
Innerchr10:58000526..58150796hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38150271
hg19150271
hg18150271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3510043
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)nsv1043534
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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