A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023385



Internal ID19112602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72350322..72393182hg38UCSC Ensembl
Innerchr7:71815307..71858167hg19UCSC Ensembl
Innerchr7:71453243..71496103hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3842861
hg1942861
hg1842861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6458n100
Supporting Variantsnssv3655700
Samples
Known GenesCALN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023385
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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