A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022440



Internal ID19111658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25260928..25350394hg38UCSC Ensembl
Innerchr9:25260926..25350392hg19UCSC Ensembl
Innerchr9:25250926..25340392hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3889467
hg1989467
hg1889467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7483n100
Supporting Variantsnssv3755866, nssv3691972, nssv3690858, nssv3691971, nssv3690860, nssv3690861, nssv3755868, nssv3691976, nssv3755865, nssv3755867, nssv3691974, nssv3690862, nssv3691975, nssv3690859, nssv3690863, nssv3691973, nssv3755869
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022440
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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