A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772128



Internal ID19313598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43906300..43906701hg38UCSC Ensembl
chr7:43945899..43946300hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074501
Supporting Variants
SamplesKWP1
Known GenesURGCP, URGCP-MRPS24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772128
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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