A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418004



Internal ID21075557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156504101..156521100hg38UCSC Ensembl
chr7:156296795..156313794hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3817000
hg1917000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151454
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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