A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704057



Internal ID15094023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:61647428..61733966hg38UCSC Ensembl
Innerchr10:63407186..63493724hg19UCSC Ensembl
Innerchr10:63077192..63163730hg18UCSC Ensembl
Innerchr10:63077192..63163730hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3886539
hg1986539
hg1886539
hg1786539
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527596
Supporting Variants
Samples
Known GenesC10orf107
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704057
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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