A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605837



Internal ID20978908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73732301..73736500hg38UCSC Ensembl
chr7:73146631..73150830hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159472
Samples
Known GenesABHD11, LINC00035
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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