A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765391



Internal ID22099862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41633302..41633519hg38UCSC Ensembl
chr17:39789554..39789771hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeOTHER delins
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438441
Supporting Variants
Samples
Known GenesKRT42P
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765391
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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