A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016699



Internal ID19105916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119139354..120348940hg38UCSC Ensembl
Innerchr6:119460519..120670086hg19UCSC Ensembl
Innerchr6:119502218..120711785hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381209587
hg191209568
hg181209568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654333
Samples
Known GenesFAM184A, LOC285762, MAN1A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016699
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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