A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513883



Internal ID20887232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67240566..67287294hg38UCSC Ensembl
chr15:67532904..67579632hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3846729
hg1946729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025445
Samples
Known GenesAAGAB, IQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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