A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025231



Internal ID18767763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106003137..106186514hg38UCSC Ensembl
Innerchr6:106451012..106634389hg19UCSC Ensembl
Innerchr6:106557705..106741082hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38183378
hg19183378
hg18183378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749507
Samples
Known GenesATG5, PRDM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025231
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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