A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700324



Internal ID15090290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110246728..110253516hg38UCSC Ensembl
Innerchr10:112006486..112013274hg19UCSC Ensembl
Innerchr10:111996476..112003264hg18UCSC Ensembl
Innerchr10:111996476..112003264hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386789
hg196789
hg186789
hg176789
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524405
Supporting Variants
Samples
Known GenesMXI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700324
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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