A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020564



Internal ID18763099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10466868..10534798hg38UCSC Ensembl
Innerchr6:10467101..10535031hg19UCSC Ensembl
Innerchr6:10575087..10643017hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3867931
hg1967931
hg1867931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n100
Supporting Variantsnssv3749026
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020564
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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