A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350041



Internal ID21007594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71203501..71204500hg38UCSC Ensembl
chr2:71430631..71431630hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089600
Samples
Known GenesPAIP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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