A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757778



Internal ID20533638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73601384..73601384hg38UCSC Ensembl
chr6:74311107..74311107hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296377
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757778
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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