A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559627



Internal ID18511222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75597408..75766272hg38UCSC Ensembl
Innerchr16:75631306..75800170hg19UCSC Ensembl
Innerchr16:74188807..74357671hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38168865
hg19168865
hg18168865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065543
Supporting Variants
Samples
Known GenesADAT1, KARS, TERF2IP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559627
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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