A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025977



Internal ID18768509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35824996..35864208hg38UCSC Ensembl
Innerchr7:35864606..35903818hg19UCSC Ensembl
Innerchr7:35831131..35870343hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3839213
hg1939213
hg1839213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643409
Samples
Known GenesSEPT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025977
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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