A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335792



Internal ID20993345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150480643..150505865hg38UCSC Ensembl
chr2:151337157..151362379hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3825223
hg1925223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078441
Samples
Known GenesRND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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