A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037092



Internal ID19126311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71732824..71816653hg38UCSC Ensembl
Innerchr11:71443870..71527699hg19UCSC Ensembl
Innerchr11:71121518..71205347hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3883830
hg1983830
hg1883830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1224n100
Supporting Variantsnssv3710655
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)nsv1037092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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