A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574109



Internal ID16361518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..949861hg38UCSC Ensembl
Innerchr17:852128..853101hg19UCSC Ensembl
Innerchr17:798878..799851hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5395n54
Supporting Variantsnssv866029, nssv866025, nssv866027, nssv866026, nssv866028
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574109
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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