A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899849



Internal ID22674984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34900706..34925269hg38UCSC Ensembl
chr6:34868483..34893046hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3824564
hg1924564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446773
Samples
Known GenesANKS1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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