A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363259



Internal ID21020812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156550277..156570184hg38UCSC Ensembl
chr3:156268066..156287973hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3819908
hg1919908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096488
Samples
Known GenesSSR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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