A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23440



Internal ID15836543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74329523..74374680hg38UCSC Ensembl
Outerchr16:74328419..74374793hg38UCSC Ensembl
Innerchr16:74363421..74408578hg19UCSC Ensembl
Outerchr16:74362317..74408691hg19UCSC Ensembl
Innerchr16:72920922..72966079hg18UCSC Ensembl
Outerchr16:72919818..72966192hg18UCSC Ensembl
Innerchr16:72920922..72966079hg17UCSC Ensembl
Outerchr16:72919818..72966192hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3846375
hg1946375
hg1846375
hg1746375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA18564
Known GenesLOC283922
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv23440
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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