A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604521



Internal ID16391930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113380637..113381782hg38UCSC Ensembl
Innerchr6:113701839..113702984hg19UCSC Ensembl
Innerchr6:113808532..113809677hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381146
hg191146
hg181146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10913n54
Supporting Variantsnssv1072072, nssv1072065, nssv1072059, nssv1072067, nssv1072061, nssv1072064, nssv1072060, nssv1072073, nssv1072070, nssv1072071, nssv1072066, nssv1072063, nssv1072069, nssv1072074, nssv1072068, nssv1072062
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604521
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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