A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034762



Internal ID19123983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8679915..8724275hg38UCSC Ensembl
Innerchr6:8680148..8724508hg19UCSC Ensembl
Innerchr6:8625147..8669507hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3844361
hg1944361
hg1844361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654754
Samples
Known GenesLOC100506207
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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