A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407191



Internal ID21064744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27684847..27902588hg38UCSC Ensembl
chr6:27652626..27870366hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38217742
hg19217741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220061
Samples
Known GenesHIST1H1B, HIST1H2AI, HIST1H2AJ, HIST1H2AK, HIST1H2AL, HIST1H2AM, HIST1H2BL, HIST1H2BM, HIST1H2BN, HIST1H2BO, HIST1H3H, HIST1H3I, HIST1H3J, HIST1H4J, HIST1H4K, HIST1H4L, LINC01012, LOC100131289
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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