A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704069



Internal ID15094035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60454406..60507710hg38UCSC Ensembl
Innerchr15:60746605..60799909hg19UCSC Ensembl
Innerchr15:58533897..58587201hg18UCSC Ensembl
Innerchr15:58533897..58587201hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3853305
hg1953305
hg1853305
hg1753305
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527607
Supporting Variants
Samples
Known GenesNARG2, RORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704069
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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