A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019145



Internal ID18761679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44345839..44453703hg38UCSC Ensembl
Innerchr6:44313576..44421440hg19UCSC Ensembl
Innerchr6:44421554..44529418hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38107865
hg19107865
hg18107865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657432
Samples
Known GenesCDC5L, MIR4642, SPATS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019145
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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