A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354581



Internal ID21012134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77947442..77985034hg38UCSC Ensembl
chr2:78174568..78212160hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3837593
hg1937593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090700
Samples
Known GenesSNAR-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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