A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504746



Internal ID20878009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67521111..67524386hg38UCSC Ensembl
chr15:67813449..67816724hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383276
hg193276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025462
Samples
Known GenesC15orf61, IQCH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504746
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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