A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591370



Internal ID16378779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119635148hg38UCSC Ensembl
Innerchr3:119351398..119353995hg19UCSC Ensembl
Innerchr3:120834088..120836685hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382598
hg192598
hg182598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971707, nssv971681, nssv971683, nssv971699, nssv971706, nssv971690, nssv971692, nssv971704, nssv971675, nssv971674, nssv971678, nssv971697, nssv971679, nssv971696, nssv971685, nssv971682, nssv971709, nssv971708, nssv971691, nssv971694, nssv971705, nssv971701, nssv971693, nssv971686, nssv971700, nssv971677, nssv971702, nssv971703, nssv971680, nssv971684, nssv971695, nssv971698, nssv971688, nssv971689, nssv971676, nssv971687
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591370
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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