A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144182



Internal ID19285663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74975150..75065387hg38UCSC Ensembl
Outerchr7:74389300..74481200hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3890238
hg1991901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3593n106
Supporting Variantsnssv3994911
SamplesKWS1
Known GenesWBSCR16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144182
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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