A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705449



Internal ID15442101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104050642..104055566hg38UCSC Ensembl
Innerchr10:105810400..105815324hg19UCSC Ensembl
Innerchr10:105800390..105805314hg18UCSC Ensembl
Innerchr10:105800390..105805314hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg384925
hg194925
hg184925
hg174925
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528782
Supporting Variants
Samples
Known GenesCOL17A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705449
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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