A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551516



Internal ID15992239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73749515..73847410hg38UCSC Ensembl
Innerchr10:75509273..75607168hg19UCSC Ensembl
Innerchr10:75179279..75277174hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3897896
hg1997896
hg1897896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750274, nssv750273
Samples
Known GenesCAMK2G, CHCHD1, FUT11, NDST2, SEC24C, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551516
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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