A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047177



Internal ID19136396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71649144..71802539hg38UCSC Ensembl
Innerchr11:71360190..71513585hg19UCSC Ensembl
Innerchr11:71037838..71191233hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38153396
hg19153396
hg18153396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1223n100
Supporting Variantsnssv3710654
Samples
Known GenesALG1L9P, FAM86C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047177
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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