A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329949



Internal ID20863103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23048001..23048800hg38UCSC Ensembl
chr1:23374494..23375293hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058604
Samples
Known GenesKDM1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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