A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025502



Internal ID19114720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1067049..1110164hg38UCSC Ensembl
Innerchr6:1067284..1110399hg19UCSC Ensembl
Innerchr6:1012284..1055399hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3843116
hg1943116
hg1843116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654713
Samples
Known GenesLOC285768
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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