A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606669



Internal ID20979740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34864114..34864545hg38UCSC Ensembl
chr7:34903726..34904157hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153087
Samples
Known GenesNPSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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