A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611489



Internal ID20984560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123695501..123696000hg38UCSC Ensembl
chr7:123335555..123336054hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150097
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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