A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966672



Internal ID18601902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26609882..26615317hg38UCSC Ensembl
Innerchr6:26610110..26615545hg19UCSC Ensembl
Innerchr6:26718089..26723524hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385436
hg195436
hg185436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758445
SamplesHGDP00665
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966672
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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