A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518549



Internal ID15099156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95500984..95577570hg38UCSC Ensembl
Innerchr6:95948860..96025446hg19UCSC Ensembl
Innerchr6:96055581..96132167hg18UCSC Ensembl
Innerchr6:96055581..96132167hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3876587
hg1976587
hg1876587
hg1776587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695992
Samples
Known GenesMANEA, MANEA-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518549
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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