A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439890



Internal ID22106067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71751318..71751386hg38UCSC Ensembl
chr10:73511075..73511143hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768207
Samples
Known GenesC10orf54, CDH23
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439890
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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