A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034427



Internal ID19123649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135001251..135033384hg38UCSC Ensembl
Innerchr6:135322389..135354522hg19UCSC Ensembl
Innerchr6:135364082..135396215hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3832134
hg1932134
hg1832134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654402
Samples
Known GenesHBS1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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