A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403355



Internal ID21060908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73283076..73294230hg38UCSC Ensembl
chr6:73992799..74003953hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811155
hg1911155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147481
Samples
Known GenesC6orf147, KHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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