A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573797



Internal ID16014520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89852908hg38UCSC Ensembl
Innerchr16:89918594..89919316hg19UCSC Ensembl
Innerchr16:88446095..88446817hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38723
hg19723
hg18723
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n54
Supporting Variantsnssv863630, nssv863632, nssv863652, nssv863619, nssv863624, nssv863654, nssv863615, nssv863647, nssv863622, nssv863651, nssv863643, nssv863623, nssv863635, nssv863633, nssv863650, nssv863636, nssv863645, nssv863644, nssv863616, nssv863639, nssv863629, nssv863638, nssv863658, nssv863655, nssv863642, nssv863656, nssv863646, nssv863627, nssv863641, nssv863628, nssv863657, nssv863614, nssv863631, nssv863618, nssv863621, nssv863617, nssv863620, nssv863649, nssv863648, nssv863626, nssv863634, nssv863625, nssv863653, nssv863640, nssv863637, nssv863613
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573797
Frequency
Sample Size17421
Observed Gain38
Observed Loss8
Observed Complex0
Frequencyn/a


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