A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525379



Internal ID15452672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30356515..30366075hg38UCSC Ensembl
Innerchr7:30396131..30405691hg19UCSC Ensembl
Innerchr7:30362656..30372216hg18UCSC Ensembl
Innerchr7:30169371..30178931hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg389561
hg199561
hg189561
hg179561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701500
Samples
Known GenesZNRF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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