A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2757037



Internal ID17871621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32484334..32518729hg38UCSC Ensembl
Innerchr6:32452111..32486506hg19UCSC Ensembl
Innerchr6:32560089..32594484hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3834396
hg1934396
hg1834396
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv981351
Supporting Variants
SamplesHGDP01284
Known GenesHLA-DRB5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2757037
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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