A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085061



Internal ID20652101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209614784..209615329hg38UCSC Ensembl
chr2:210479508..210480053hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350945
Supporting Variants
Samples
Known GenesMAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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