A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526129



Internal ID15453422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168310490..168319244hg38UCSC Ensembl
Innerchr6:168711170..168719924hg19UCSC Ensembl
Innerchr6:168454019..168462773hg18UCSC Ensembl
Innerchr6:168529726..168538480hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388755
hg198755
hg188755
hg178755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702383
Samples
Known GenesDACT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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