A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696134



Internal ID15086100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1166695..1168138hg38UCSC Ensembl
Innerchr10:1212635..1214078hg19UCSC Ensembl
Innerchr10:1202635..1204078hg18UCSC Ensembl
Innerchr10:1202635..1204078hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381444
hg191444
hg181444
hg171444
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517780
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696134
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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