A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578388



Internal ID16365797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2699587..2702401hg38UCSC Ensembl
Innerchr19:2699585..2702399hg19UCSC Ensembl
Innerchr19:2650585..2653399hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382815
hg192815
hg182815
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv892084, nssv892075, nssv892080, nssv892078, nssv892082, nssv892081, nssv892079, nssv892083, nssv892076, nssv892077, nssv892085
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578388
Frequency
Sample Size17421
Observed Gain3
Observed Loss8
Observed Complex0
Frequencyn/a


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