A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3773025



Internal ID18964349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143380906..143381507hg38UCSC Ensembl
chr7:143077999..143078600hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075065
Supporting Variants
SamplesKWP1
Known GenesZYX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3773025
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer