A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559820



Internal ID18858101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81144088..81233236hg38UCSC Ensembl
Innerchr16:81177693..81266841hg19UCSC Ensembl
Innerchr16:79735194..79824342hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3889149
hg1989149
hg1889149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056584
Supporting Variants
Samples
Known GenesPKD1L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559820
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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