A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023619



Internal ID19112836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88999845..89048870hg38UCSC Ensembl
Innerchr6:89709564..89758589hg19UCSC Ensembl
Innerchr6:89766283..89815308hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3849026
hg1949026
hg1849026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6088n100
Supporting Variantsnssv3648952, nssv3648950, nssv3648951
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)nsv1023619
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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