A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018932



Internal ID19108149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140458389..140542009hg38UCSC Ensembl
Innerchr6:140779526..140863146hg19UCSC Ensembl
Innerchr6:140821219..140904839hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3883621
hg1983621
hg1883621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6156n100
Supporting Variantsnssv3654424, nssv3654427, nssv3654426, nssv3654425
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)nsv1018932
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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