A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610086



Internal ID20983157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127314035..127314491hg38UCSC Ensembl
chr6:127635180..127635636hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137669
Samples
Known GenesECHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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