A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408714



Internal ID21066267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161382961..161385710hg38UCSC Ensembl
chr5:160809967..160812716hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126568
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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