A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710644



Internal ID18662239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71588129..71816850hg38UCSC Ensembl
Innerchr11:71299175..71527896hg19UCSC Ensembl
Innerchr11:70976823..71205544hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38228722
hg19228722
hg18228722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041027
Supporting Variants
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710644
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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