A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056481



Internal ID19145700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42782600..42858488hg38UCSC Ensembl
Innerchr19:43286752..43362640hg19UCSC Ensembl
Innerchr19:47978592..48054480hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3875889
hg1975889
hg1875889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3562n100
Supporting Variantsnssv3568929, nssv3568923, nssv3722890, nssv3568925, nssv3568922, nssv3568926, nssv3568916, nssv3722889, nssv3568927, nssv3722891, nssv3568921, nssv3568928, nssv3568919, nssv3722892, nssv3568930, nssv3568918, nssv3568920, nssv3568917, nssv3568924
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056481
Frequency
Sample Size11257
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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