A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017380



Internal ID18759914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5007636..5152317hg38UCSC Ensembl
Innerchr6:5007870..5152551hg19UCSC Ensembl
Innerchr6:4952869..5097550hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38144682
hg19144682
hg18144682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654734
Samples
Known GenesLYRM4, MIR3691, PPP1R3G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017380
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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