A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335624



Internal ID20993177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237268101..237271200hg38UCSC Ensembl
chr2:238176744..238179843hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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