A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752221



Internal ID16046177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86366299..86367707hg38UCSC Ensembl
Innerchr10:88126056..88127464hg19UCSC Ensembl
Innerchr10:88116036..88117444hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381409
hg191409
hg181409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551779
Supporting Variants
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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