A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057261



Internal ID19146480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35475416hg38UCSC Ensembl
Innerchr16:34466559..34709787hg19UCSC Ensembl
Innerchr16:34324060..34567288hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38243229
hg19243229
hg18243229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3556108
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057261
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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