A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351156



Internal ID21008709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70355511..70355906hg38UCSC Ensembl
chr2:70582643..70583038hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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