A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678770



Internal ID15068736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74248145..74612279hg38UCSC Ensembl
Innerchr10:76007903..76372037hg19UCSC Ensembl
Innerchr10:75677909..76042043hg18UCSC Ensembl
Innerchr10:75677909..76042043hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38364135
hg19364135
hg18364135
hg17364135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515824
Supporting Variants
Samples
Known GenesADK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678770
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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