A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035530



Internal ID19124749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93380945..93415782hg38UCSC Ensembl
Innerchr11:93114111..93148948hg19UCSC Ensembl
Innerchr11:92753759..92788596hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3834838
hg1934838
hg1834838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503882
Samples
Known GenesCCDC67
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035530
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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