A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438870



Internal ID22105047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56776934..56777273hg38UCSC Ensembl
chr1:57242607..57242946hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764980
Samples
Known GenesC1orf168
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438870
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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