A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655380



Internal ID15045346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28278878..28291040hg38UCSC Ensembl
Innerchr10:28567807..28579969hg19UCSC Ensembl
Innerchr10:28607813..28619975hg18UCSC Ensembl
Innerchr10:28607813..28619975hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3812163
hg1912163
hg1812163
hg1712163
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515548
Supporting Variants
Samples
Known GenesMIR8086, MPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655380
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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