A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718921



Internal ID19017202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14885100..15322641hg38UCSC Ensembl
Innerchr16:14978957..15416498hg19UCSC Ensembl
Innerchr16:14886458..15323999hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38437542
hg19437542
hg18437542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038955
Supporting Variants
Samples
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, NOMO1, NPIPA1, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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