A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034095



Internal ID19123317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57237244..57298010hg38UCSC Ensembl
Innerchr6:57102042..57162808hg19UCSC Ensembl
Innerchr6:57210001..57270767hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3860767
hg1960767
hg1860767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657504
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)nsv1034095
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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