A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353174



Internal ID21010727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85551505..85552176hg38UCSC Ensembl
chr2:85778628..85779299hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091139
Samples
Known GenesGGCX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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