A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006774



Internal ID18749305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108522528..108559230hg38UCSC Ensembl
Innerchr3:108241375..108278077hg19UCSC Ensembl
Innerchr3:109724065..109760767hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3836703
hg1936703
hg1836703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604398
Samples
Known GenesKIAA1524, MYH15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006774
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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