A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342604



Internal ID21000157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84245585..84300206hg38UCSC Ensembl
chr2:84472709..84527330hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3854622
hg1954622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092197
Samples
Known GenesFUNDC2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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