A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061070



Internal ID18803601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70117645hg38UCSC Ensembl
Innerchr16:70049784..70151548hg19UCSC Ensembl
Innerchr16:68607285..68709049hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38101765
hg19101765
hg18101765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3002n100
Supporting Variantsnssv3559498
Samples
Known GenesMIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061070
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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