A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024700



Internal ID19113917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149265292..149313916hg38UCSC Ensembl
Innerchr7:148962383..149011007hg19UCSC Ensembl
Innerchr7:148593316..148641940hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3848625
hg1948625
hg1848625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674236
Samples
Known GenesLOC155060, ZNF783
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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