A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516946



Internal ID15444239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45892681..46184668hg38UCSC Ensembl
Innerchr14:46361884..46653871hg19UCSC Ensembl
Innerchr14:45431634..45723621hg18UCSC Ensembl
Innerchr14:45431634..45723621hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38291988
hg19291988
hg18291988
hg17291988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702268, nssv678368, nssv661900, nssv700882, nssv668811, nssv690796, nssv677124, nssv696229, nssv705691, nssv653596, nssv687322, nssv660928, nssv670042, nssv689213, nssv660380, nssv696827, nssv681390, nssv665094, nssv675334, nssv664121, nssv675162, nssv653482, nssv664160, nssv651936, nssv660536, nssv679111, nssv676320, nssv674020, nssv686201, nssv653389, nssv687172, nssv686639, nssv685291, nssv663777, nssv684020
Samples
Known GenesLINC00871
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516946
Frequency
Sample Size2026
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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