A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617066



Internal ID20990137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75656601..75658200hg38UCSC Ensembl
chr7:75285919..75287518hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158119
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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