A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022705



Internal ID19111923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50376576..50426391hg38UCSC Ensembl
Innerchr6:50344289..50394104hg19UCSC Ensembl
Innerchr6:50452248..50502063hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3849816
hg1949816
hg1849816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657453
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022705
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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