A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351857



Internal ID21009410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195738101..195761700hg38UCSC Ensembl
chr2:196602825..196626424hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3823600
hg1923600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081927
Samples
Known GenesDNAH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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