A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022062



Internal ID18764596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135392330..135435396hg38UCSC Ensembl
Innerchr6:135713468..135756534hg19UCSC Ensembl
Innerchr6:135755161..135798227hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3843067
hg1943067
hg1843067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654404
Samples
Known GenesAHI1, MIR548H4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022062
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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