A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396134



Internal ID21053687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10787814..10829086hg38UCSC Ensembl
chr6:10788047..10829319hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3841273
hg1941273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136962
Samples
Known GenesMAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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