A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664889



Internal ID15054855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74612279..74614146hg38UCSC Ensembl
Innerchr10:76372037..76373904hg19UCSC Ensembl
Innerchr10:76042043..76043910hg18UCSC Ensembl
Innerchr10:76042043..76043910hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381868
hg191868
hg181868
hg171868
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)nssv664889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer