A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321852



Internal ID20854960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247534329..247538067hg38UCSC Ensembl
chr1:247697631..247701369hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg383739
hg193739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060167
Samples
Known GenesGCSAML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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