A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342257



Internal ID20999810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64917601..64926600hg38UCSC Ensembl
chr2:65144735..65153734hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089324
Samples
Known GenesLOC400958
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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