A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927292



Internal ID21347362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6979792..6979845hg38UCSC Ensembl
chr1:7039852..7039905hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180909
SamplesHG002
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927292
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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