A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705412



Internal ID15442064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45529172..45580787hg38UCSC Ensembl
Innerchr10:46024620..46076235hg19UCSC Ensembl
Innerchr10:45344626..45396241hg18UCSC Ensembl
Innerchr10:45344626..45396241hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3851616
hg1951616
hg1851616
hg1751616
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528750
Supporting Variants
Samples
Known GenesMARCH8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705412
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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