A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046807



Internal ID19136026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116346368..116402574hg38UCSC Ensembl
Innerchr10:118105880..118162086hg19UCSC Ensembl
Innerchr10:118095870..118152076hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3856207
hg1956207
hg1856207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509271
Samples
Known GenesCCDC172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046807
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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