A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037879



Internal ID93004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319733..92322984hg38UCSC Ensembl
chr10:94079490..94082741hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383252
hg193252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482420
Supporting Variants
Samples
Known GenesMARCH5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004705


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