A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019895



Internal ID19109113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1832702..1882201hg38UCSC Ensembl
Innerchr6:1832936..1882435hg19UCSC Ensembl
Innerchr6:1777935..1827434hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849500
hg1949500
hg1849500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654719
Samples
Known GenesGMDS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019895
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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