A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685614



Internal ID15075580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74248145..74614146hg38UCSC Ensembl
Innerchr10:76007903..76373904hg19UCSC Ensembl
Innerchr10:75677909..76043910hg18UCSC Ensembl
Innerchr10:75677909..76043910hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38366002
hg19366002
hg18366002
hg17366002
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)nssv685614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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