A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017541



Internal ID19106758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8589683..8722484hg38UCSC Ensembl
Innerchr6:8589916..8722717hg19UCSC Ensembl
Innerchr6:8534915..8667716hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38132802
hg19132802
hg18132802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5915n100
Supporting Variantsnssv3654751
Samples
Known GenesHULC, LOC100506207
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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