A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517171



Internal ID15444464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14215597..14272059hg38UCSC Ensembl
Innerchr2:14355721..14412183hg19UCSC Ensembl
Innerchr2:14273172..14329634hg18UCSC Ensembl
Innerchr2:14306319..14362781hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3856463
hg1956463
hg1856463
hg1756463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692245, nssv675111, nssv652217, nssv688577, nssv676586, nssv653922, nssv671175, nssv693984, nssv692189, nssv678552
Samples
Known GenesLINC00276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517171
Frequency
Sample Size2026
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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