A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603728



Internal ID20976799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47668931..47793856hg38UCSC Ensembl
chr7:47708529..47833454hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38124926
hg19124926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155441
Samples
Known GenesLINC00525, PKD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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