A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517011



Internal ID15097618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119039314..119046720hg38UCSC Ensembl
Innerchr1:119581937..119589343hg19UCSC Ensembl
Innerchr1:119383460..119390866hg18UCSC Ensembl
Innerchr1:119293979..119301385hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg387407
hg197407
hg187407
hg177407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16n21
Supporting Variantsnssv653612, nssv683910
Samples
Known GenesWARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517011
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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