A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076923



Internal ID19317870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73667769..73668270hg38UCSC Ensembl
chr7:73082099..73082600hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762316
SamplesKWP1
Known GenesVPS37D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076923
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