A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522955



Internal ID15450248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78463408..78466555hg38UCSC Ensembl
Innerchr7:78092725..78095872hg19UCSC Ensembl
Innerchr7:77930661..77933808hg18UCSC Ensembl
Innerchr7:77737376..77740523hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383148
hg193148
hg183148
hg173148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698624
Samples
Known GenesMAGI2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522955
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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