A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517544



Internal ID15444837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173511984..173583247hg38UCSC Ensembl
Innerchr3:173229774..173301037hg19UCSC Ensembl
Innerchr3:174712468..174783731hg18UCSC Ensembl
Innerchr3:174712476..174783739hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3871264
hg1971264
hg1871264
hg1771264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv304n21
Supporting Variantsnssv688487, nssv669534, nssv669729, nssv659130, nssv669851, nssv690243, nssv681359, nssv692154, nssv655241, nssv653287, nssv663045, nssv660871, nssv652723, nssv670937, nssv667179, nssv686624, nssv652514, nssv657538, nssv688010, nssv682464, nssv665693, nssv677560, nssv670692, nssv666973, nssv692634, nssv680597, nssv676156, nssv692359, nssv703655, nssv658176, nssv652324, nssv654780, nssv670967
Samples
Known GenesNLGN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517544
Frequency
Sample Size2026
Observed Gain33
Observed Loss0
Observed Complex0
Frequencyn/a


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