A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001877



Internal ID19091094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062181..13140112hg38UCSC Ensembl
Innerchr2:13202306..13280237hg19UCSC Ensembl
Innerchr2:13119757..13197688hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3877932
hg1977932
hg1877932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3718n100
Supporting Variantsnssv3726777, nssv3577014, nssv3577029, nssv3577019, nssv3577025, nssv3726774, nssv3726765, nssv3726784, nssv3726771, nssv3577018, nssv3577016, nssv3577010, nssv3726775, nssv3726767, nssv3726768, nssv3726783, nssv3577012, nssv3577022, nssv3726772, nssv3726769, nssv3577021, nssv3726776, nssv3577008, nssv3577027, nssv3726766, nssv3726785, nssv3577024, nssv3726780, nssv3577011, nssv3577013, nssv3577023, nssv3577015, nssv3726773, nssv3577017, nssv3577007, nssv3577028, nssv3726778, nssv3726782, nssv3577020, nssv3577026, nssv3726779, nssv3577009, nssv3726781, nssv3726770, nssv3577006
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)nsv1001877
Frequency
Sample Size11257
Observed Gain45
Observed Loss0
Observed Complex0
Frequencyn/a


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