A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772140



Internal ID18960551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437697..37438009hg38UCSC Ensembl
chr7:37477300..37477612hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074496
Supporting Variants
SamplesKWP1
Known GenesELMO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772140
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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