A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764897



Internal ID19313423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127250845..127255146hg38UCSC Ensembl
chr7:126890899..126895200hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg384302
hg194302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075058
Supporting Variants
SamplesKWP1
Known GenesGRM8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764897
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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