A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515536



Internal ID15096143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35728624..35750059hg38UCSC Ensembl
Innerchr19:36219525..36240960hg19UCSC Ensembl
Innerchr19:40911365..40932800hg18UCSC Ensembl
Innerchr19:40911365..40932800hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821436
hg1921436
hg1821436
hg1721436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674588, nssv670781, nssv704831, nssv663674, nssv690309, nssv658673, nssv663852, nssv691805
Samples
Known GenesIGFLR1, KMT2B, LIN37, PSENEN, U2AF1L4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515536
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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