A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897903



Internal ID22673013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2310810..2318043hg38UCSC Ensembl
chr6:2311044..2318277hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387234
hg197234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437700
Samples
Known GenesGMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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