A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021744



Internal ID19110962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120465469..120548044hg38UCSC Ensembl
Innerchr6:120786615..120869190hg19UCSC Ensembl
Innerchr6:120828314..120910889hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3882576
hg1982576
hg1882576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654338
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)nsv1021744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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