A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718830



Internal ID18670425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1784723..1866102hg38UCSC Ensembl
Innerchr16:1834724..1916103hg19UCSC Ensembl
Innerchr16:1774725..1856104hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3881380
hg1981380
hg1881380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042986
Supporting Variants
Samples
Known GenesFAHD1, HAGH, IGFALS, MEIOB, NUBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718830
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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