A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030509



Internal ID19119728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153565024..153721056hg38UCSC Ensembl
Innerchr6:153886159..154042191hg19UCSC Ensembl
Innerchr6:153927852..154083884hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38156033
hg19156033
hg18156033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654477
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)nsv1030509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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