A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342972



Internal ID21000525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212756701..212785200hg38UCSC Ensembl
chr2:213621425..213649924hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3828500
hg1928500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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